American Journal of Medical Genetics

Cover image for American Journal of Medical Genetics

Special Issue: X-Linked Mental Retardation 4

1 February - 1 March 1991

Volume 38, Issue 2-3

Pages fmi–fmi, 158–516

Currently known as: American Journal of Medical Genetics Part A

  1. Masthead

    1. Top of page
    2. Masthead
    3. Introduction
    4. Nosology
    5. Letter to the Editor
    6. Nosology
    7. Letter to the Editor
    8. Clinical Anthropometry
    9. Letter to the Editor
    10. Linkage, Carrier, Molecular, and Genetic Studies
    11. Letter to the Editor
    12. Linkage, Carrier, Molecular, and Genetic Studies
    13. Cytogenetics and Somatic Cell Genetics
    14. Letter to the Editor
    15. Prenatal Diagnosis
    16. Psychology, Neurology, and Neuropathology
    17. Letter to the Editor
    18. Psychology, Neurology, and Neuropathology
    19. Abstracts
    1. Masthead (page fmi)

      Article first published online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320380201

  2. Introduction

    1. Top of page
    2. Masthead
    3. Introduction
    4. Nosology
    5. Letter to the Editor
    6. Nosology
    7. Letter to the Editor
    8. Clinical Anthropometry
    9. Letter to the Editor
    10. Linkage, Carrier, Molecular, and Genetic Studies
    11. Letter to the Editor
    12. Linkage, Carrier, Molecular, and Genetic Studies
    13. Cytogenetics and Somatic Cell Genetics
    14. Letter to the Editor
    15. Prenatal Diagnosis
    16. Psychology, Neurology, and Neuropathology
    17. Letter to the Editor
    18. Psychology, Neurology, and Neuropathology
    19. Abstracts
    1. Conference report: Fourth International Workshop on the Fragile X and X-linked mental retardation (pages 158–172)

      Dr. W. Ted Brown, Ed Jenkins, Giovanni Neri, Herbert Lubs, Lawrence R. Shapiro, Kay E. Davies, Stephanie Sherman, Randi Hagerman and Charles Laird

      Article first published online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320380202

    2. You have free access to this content
  3. Nosology

    1. Top of page
    2. Masthead
    3. Introduction
    4. Nosology
    5. Letter to the Editor
    6. Nosology
    7. Letter to the Editor
    8. Clinical Anthropometry
    9. Letter to the Editor
    10. Linkage, Carrier, Molecular, and Genetic Studies
    11. Letter to the Editor
    12. Linkage, Carrier, Molecular, and Genetic Studies
    13. Cytogenetics and Somatic Cell Genetics
    14. Letter to the Editor
    15. Prenatal Diagnosis
    16. Psychology, Neurology, and Neuropathology
    17. Letter to the Editor
    18. Psychology, Neurology, and Neuropathology
    19. Abstracts
    1. XLMR genes: Update 1990 (pages 186–189)

      Giovanni Neri, Fiorella Gurrieri, Andreas Gal and Herbert A. Lubs

      Article first published online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320380204

    2. Computerized approach to X-linked mental retardation syndromes (pages 190–199)

      J. Fernando Arena and Herbert A. Lubs

      Article first published online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320380205

    3. New X-linked mental retardation disorder with Dandy-Walker malformation, basal ganglia disease, and seizures (pages 200–207)

      Anjana L. Pettigrew, Laird G. Jackson and David H. Ledbetter

      Article first published online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320380206

    4. Gene for non-specific X-linked mental retardation maps in the pericentromeric region (pages 224–227)

      Christine Samanns, Regine Albrecht, Meinhard Neugebauer, Giovanni Neri and Andreas Gal

      Article first published online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320380210

    5. X-linked mental retardation with marfanoid habitus: First report of four Italian patients (pages 228–232)

      F. Lalatta, E. Livini, A. Selicorni, V. Briscioli, A. Vita, F. Lugo, M. Zollino, F. Gurrieri and G. Neri

      Article first published online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320380211

  4. Letter to the Editor

    1. Top of page
    2. Masthead
    3. Introduction
    4. Nosology
    5. Letter to the Editor
    6. Nosology
    7. Letter to the Editor
    8. Clinical Anthropometry
    9. Letter to the Editor
    10. Linkage, Carrier, Molecular, and Genetic Studies
    11. Letter to the Editor
    12. Linkage, Carrier, Molecular, and Genetic Studies
    13. Cytogenetics and Somatic Cell Genetics
    14. Letter to the Editor
    15. Prenatal Diagnosis
    16. Psychology, Neurology, and Neuropathology
    17. Letter to the Editor
    18. Psychology, Neurology, and Neuropathology
    19. Abstracts
    1. X-linked mental retardation with Marfanoid habitus (page 233)

      J. P. Fryns

      Article first published online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320380212

  5. Nosology

    1. Top of page
    2. Masthead
    3. Introduction
    4. Nosology
    5. Letter to the Editor
    6. Nosology
    7. Letter to the Editor
    8. Clinical Anthropometry
    9. Letter to the Editor
    10. Linkage, Carrier, Molecular, and Genetic Studies
    11. Letter to the Editor
    12. Linkage, Carrier, Molecular, and Genetic Studies
    13. Cytogenetics and Somatic Cell Genetics
    14. Letter to the Editor
    15. Prenatal Diagnosis
    16. Psychology, Neurology, and Neuropathology
    17. Letter to the Editor
    18. Psychology, Neurology, and Neuropathology
    19. Abstracts
    1. Gene localization in a family with X-linked syndromal mental retardation (Prieto syndrome) (pages 234–239)

      Anke Watty, Félix Prieto, Magdalena Beneyto, Meinhard Neugebauer and Andreas Gal

      Article first published online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320380213

    2. Linkage analysis in a large family with nonspecific X-linked mental retardation (pages 240–243)

      Dr. I. A. Glass, E. M. White, M. J. Pope, L. A. Pirrit, F. Cockburn and J. M. Connor

      Article first published online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320380214

    3. Simpson-Golabi-Behmel syndrome with severe cardiac arrhythmias (pages 244–247)

      Dr. Rainer König, Sigrun Fuchs, Christoph Kern and Ulrich Langenbeck

      Article first published online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320380215

  6. Letter to the Editor

    1. Top of page
    2. Masthead
    3. Introduction
    4. Nosology
    5. Letter to the Editor
    6. Nosology
    7. Letter to the Editor
    8. Clinical Anthropometry
    9. Letter to the Editor
    10. Linkage, Carrier, Molecular, and Genetic Studies
    11. Letter to the Editor
    12. Linkage, Carrier, Molecular, and Genetic Studies
    13. Cytogenetics and Somatic Cell Genetics
    14. Letter to the Editor
    15. Prenatal Diagnosis
    16. Psychology, Neurology, and Neuropathology
    17. Letter to the Editor
    18. Psychology, Neurology, and Neuropathology
    19. Abstracts
    1. Cutis verticis gyrata and chromosomal fragile sites (pages 249–250)

      S. A. Musumeci, R. Ferri, M. Viglianesi, M. Elia, R. M. Ragusa and P. Bergonzi

      Article first published online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320380217

  7. Clinical Anthropometry

    1. Top of page
    2. Masthead
    3. Introduction
    4. Nosology
    5. Letter to the Editor
    6. Nosology
    7. Letter to the Editor
    8. Clinical Anthropometry
    9. Letter to the Editor
    10. Linkage, Carrier, Molecular, and Genetic Studies
    11. Letter to the Editor
    12. Linkage, Carrier, Molecular, and Genetic Studies
    13. Cytogenetics and Somatic Cell Genetics
    14. Letter to the Editor
    15. Prenatal Diagnosis
    16. Psychology, Neurology, and Neuropathology
    17. Letter to the Editor
    18. Psychology, Neurology, and Neuropathology
    19. Abstracts
    1. Fragile X screening program in New York State (pages 251–255)

      Sarah L. Nolin, Donald A. Snider, Edmund C. Jenkins, W. Ted Brown, Michael Krawczun, Daniel Stetka, George Houck Jr., Carl S. Dobkin, Gloria Strong, Gail Smith-Dobransky, Arnold Victor, Kevin Hughes, Donna Kimpton, Anne Little, U. Nagaraja, Barbara Kenefick and Connie Sullivan

      Article first published online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320380218

    2. Clinical screening score for the fragile X (Martin-Bell) syndrome (pages 256–259)

      Sue Laing, Michael Partington, Hazel Robinson and Gillian Turner

      Article first published online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320380219

    3. Anthropometric comparison of mentally retarded males with and without the fragile X syndrome (pages 260–268)

      Merlin G. Butler, G. Andrew Allen, Judy L. Haynes, Dharmdeo N. Singh, Michael S. Watson and W. Roy Breg

      Article first published online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320380220

    4. Heterozygous fragile X female: Historical, physical, cognitive, and cytogenetic features (pages 269–274)

      Amy Cronister, Rebecca Schreiner, Michael Wittenberger, Khaled Amiri, Keri Harris and Randi J. Hagerman

      Article first published online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320380221

    5. Martin–Bell syndrome segregating in a large kindred with normal transmitting males: Clinical, cytogenetic, and linkage study (pages 275–282)

      Virginia P. Johnson, Nancy J. Carpenter and Patricia A. Skorey

      Article first published online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320380222

    6. Fragile X checklist (pages 283–287)

      Randi J. Hagerman, Khaled Amiri and Amy Cronister

      Article first published online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320380223

  8. Letter to the Editor

    1. Top of page
    2. Masthead
    3. Introduction
    4. Nosology
    5. Letter to the Editor
    6. Nosology
    7. Letter to the Editor
    8. Clinical Anthropometry
    9. Letter to the Editor
    10. Linkage, Carrier, Molecular, and Genetic Studies
    11. Letter to the Editor
    12. Linkage, Carrier, Molecular, and Genetic Studies
    13. Cytogenetics and Somatic Cell Genetics
    14. Letter to the Editor
    15. Prenatal Diagnosis
    16. Psychology, Neurology, and Neuropathology
    17. Letter to the Editor
    18. Psychology, Neurology, and Neuropathology
    19. Abstracts
    1. Fragile X syndrome (Martin-Bell Syndrome) in China (pages 288–289)

      Dr. Y. Zhao, Y. Shen, Y. Liu, J.-C. Zhang, L.-Z. Ye, S.-W. Ma, W. H. Y. Lo, G.-Y. Wu, Z.-Y. Cheng and X.-Z. Zhang

      Article first published online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320380224

    2. A girl with the Lujan-Fryns Syndrome (pages 290–291)

      Fiorella Gurrieri and Prof. Giovanni Neri

      Article first published online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320380225

  9. Linkage, Carrier, Molecular, and Genetic Studies

    1. Top of page
    2. Masthead
    3. Introduction
    4. Nosology
    5. Letter to the Editor
    6. Nosology
    7. Letter to the Editor
    8. Clinical Anthropometry
    9. Letter to the Editor
    10. Linkage, Carrier, Molecular, and Genetic Studies
    11. Letter to the Editor
    12. Linkage, Carrier, Molecular, and Genetic Studies
    13. Cytogenetics and Somatic Cell Genetics
    14. Letter to the Editor
    15. Prenatal Diagnosis
    16. Psychology, Neurology, and Neuropathology
    17. Letter to the Editor
    18. Psychology, Neurology, and Neuropathology
    19. Abstracts
    1. Detection of fragile X non-penetrant males by DNA marker analysis (pages 292–297)

      W. Ted Brown, Anne Gross, Ponmani Goonewardena, Charles Ferrando, Carl Dobkin and Edmund C. Jenkins

      Article first published online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320380226

    2. Linkage analysis in the fragile X syndrome using multiple distal Xq polymorphic DNA markers (pages 298–304)

      Dr. I. A. Glass, L. A. Pirrit, E. M. White, M. V. Bell, K. E. Davies, F. Cockburn and J. M. Connor

      Article first published online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320380227

    3. DNA-based genetic testing in fifty fragile X families (pages 305–310)

      P. D. Murphy, M. S. Watson, L. R. Shapiro, P. L. Wilmot and W. R. Breg

      Article first published online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320380228

    4. DNA linkage analysis of 26 families with fragile X syndrome (pages 311–318)

      Nancy J. Carpenter

      Article first published online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320380229

    5. Carrier detection of the fragile X syndrome using flanking loci DXS98, DXS105, and DXS304 (pages 319–321)

      Niklas Dahl, Helena Malmgren, Ulf Pettersson, Gösta Holmgren, Eva Seemanová and Karl-Henrik Gustavson

      Article first published online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320380230

    6. Linkage analysis of the fragile X syndrome using a new DNA marker U6.2 defining locus DXS304 (pages 322–327)

      Ponmani Goonewardena, Dr. W. Ted Brown, Anne C. Gross, Charles Ferrando, Carl Dobkin, Valentino Romano, Paolo Bosco, Nadia Ceratto, Ulf Pettersson and Niklas Dahl

      Article first published online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320380231

    7. Multipoint linkage analysis of DXS369 and DXS304 in fragile X families (pages 328–331)

      B. A. van Oost, A. Smits, J. C. F. M. Dreesen, D. Smeets, L. Perdon, C. A. van Bennekom, N. Dahl, E. Bakker and B. A. Oostra

      Article first published online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320380232

    8. Mapping of a new RFLP marker RN1 (DXS369) close to the fragile site FRAXA on Xq27–q28 (pages 332–335)

      Dr. B. A. Oostra, D. F. Majoor-Krakauer, J. O. van Hemel, E. Bakker, D. F. Callen, M. Schmidt and B. A. van Oost

      Article first published online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320380233

    9. New polymorphism and a new chromosome breakpoint establish the physical and genetic mapping of DXS369 in the DXS98-FRAXA Interval (pages 336–342)

      I. Oberlé, A. Vincent, N. Abbadi, F. Rousseau, P. E. Hupkes, M. C. Hors-Cayla, S. Gilgenkrantz, B. A. Oostra and J. L. Mandel

      Article first published online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320380234

    10. Linkage in fragile X families of three distal flanking markers: ST14, DX13, and F8 (pages 343–346)

      W. Ted Brown, Anne C. Gross, Ponmani Goonewardena, Charles Ferrando, Carl Dobkin and Edmund C. Jenkins

      Article first published online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320380235

  10. Letter to the Editor

    1. Top of page
    2. Masthead
    3. Introduction
    4. Nosology
    5. Letter to the Editor
    6. Nosology
    7. Letter to the Editor
    8. Clinical Anthropometry
    9. Letter to the Editor
    10. Linkage, Carrier, Molecular, and Genetic Studies
    11. Letter to the Editor
    12. Linkage, Carrier, Molecular, and Genetic Studies
    13. Cytogenetics and Somatic Cell Genetics
    14. Letter to the Editor
    15. Prenatal Diagnosis
    16. Psychology, Neurology, and Neuropathology
    17. Letter to the Editor
    18. Psychology, Neurology, and Neuropathology
    19. Abstracts
    1. RFLP analysis in 5 Sicilian families with the fragile X syndrome (pages 347–348)

      Valentino Romano, Gaetano Mascali, Valeria Chiaveta, Rosa Maria Ragusa, Cosimo Barletta, Corrado Romano, Florindo Mollica, Teresa Mattina, Anne Gross, W. Ted Brown, Carl S. Dobkin and Charles Ferrando

      Article first published online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320380236

  11. Linkage, Carrier, Molecular, and Genetic Studies

    1. Top of page
    2. Masthead
    3. Introduction
    4. Nosology
    5. Letter to the Editor
    6. Nosology
    7. Letter to the Editor
    8. Clinical Anthropometry
    9. Letter to the Editor
    10. Linkage, Carrier, Molecular, and Genetic Studies
    11. Letter to the Editor
    12. Linkage, Carrier, Molecular, and Genetic Studies
    13. Cytogenetics and Somatic Cell Genetics
    14. Letter to the Editor
    15. Prenatal Diagnosis
    16. Psychology, Neurology, and Neuropathology
    17. Letter to the Editor
    18. Psychology, Neurology, and Neuropathology
    19. Abstracts
    1. Linkage relationships between DXS105, DXS98, and other polymorphic DNA markers flanking the fragile X locus (pages 349–353)

      Nancy J. Carpenter, Stephen N. Thibodeau and W. Ted Brown

      Article first published online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320380237

    2. Mapping of a cerebellar degeneration related protein and DXS304 around the fragile site (pages 354–356)

      M. C. Hirst, M. V. Bell, R. N. MacKinnon, J. E. V. Watson, D. Callen, G. Sutherland, N. Dahl, M. N. Patterson, C. Schwartz, D. Ledbetter, S. Ledbetter and K. E. Davies

      Article first published online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320380238

    3. Physical and genetic mapping of the CDR gene with particular reference to its position with respect to the FRAXA site (pages 357–362)

      Marcello Siniscalco, Isabelle Oberlé, Paola Melis, Becky Alhadeff, Jeff Murray, Giorgio Filippi, Tiziana Mattioni, Yao-Tseng Chen, Henry Furneaux, Lloyd J. Old and Jerome B. Posner

      Article first published online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320380239

    4. Fragile X families in a Northern Swedish County: A genealogical study of possibly affected individuals in the nineteenth century (pages 363–366)

      Ulf Drugge, Hans K:son Blomquist, Karl-Henrik Gustavson and Gösta Holmgren

      Article first published online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320380240

    5. Transmission of mental retardation with fragile X site by two normal transmitter brothers (pages 367–369)

      Marie-Christine Pellissier, Marie-Antoinette Voelckel, Caroline Piquet, Marie-Geneviève Mattei and Dr. Jean-François Mattei

      Article first published online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320380241

    6. Cytogenetically negative, linkage positive “fragile X” syndrome (pages 370–373)

      Susan Sklower Brooks, Ira Cohen, Charles Ferrando, Edmund C. Jenkins, W. Ted Brown and Carl Dobkin

      Article first published online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320380242

    7. Fragile X syndrome in an extended family with special reference to an affected male with Klinefelter Syndrome (pages 374–377)

      Marie-Antoinette Voelckel, Marie-Christine Pellissier, Caroline Piquet, Catherine N'Guyen, Irène Boccaccio, Nicole Philip and Dr. Jean-François Mattei

      Article first published online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320380243

    8. Polymerase chain reaction detection of the Dde I polymorphism in the factor 9 gene for fragile X linkage analysis (pages 378–379)

      Carl S. Dobkin, M. Catherine Driscoll and Charles Ferrando

      Article first published online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320380244

    9. Molecular characterization of a DNA probe, U6.2, located close to the fragile X locus (pages 380–383)

      Robert Pergolizzi, W. Ted Brown, Ponmani Goonewardena, Romal Bhan, Carl Dobkin, Niklas Dahl and Ulf Pettersson

      Article first published online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320380245

    10. Cloning the ends of size selected Sfi I fragments (pages 384–390)

      Sarah L. Nolin and Carl S. Dobkin

      Article first published online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320380246

  12. Cytogenetics and Somatic Cell Genetics

    1. Top of page
    2. Masthead
    3. Introduction
    4. Nosology
    5. Letter to the Editor
    6. Nosology
    7. Letter to the Editor
    8. Clinical Anthropometry
    9. Letter to the Editor
    10. Linkage, Carrier, Molecular, and Genetic Studies
    11. Letter to the Editor
    12. Linkage, Carrier, Molecular, and Genetic Studies
    13. Cytogenetics and Somatic Cell Genetics
    14. Letter to the Editor
    15. Prenatal Diagnosis
    16. Psychology, Neurology, and Neuropathology
    17. Letter to the Editor
    18. Psychology, Neurology, and Neuropathology
    19. Abstracts
    1. Guidelines for the Preparation and Analysis of the Fragile X Chromosome in Lymphocytes (pages 400–403)

      P. B. Jacky, Y. R. Ahuja, K. Anyane-Yeboa, W. R. Breg, N. J. Carpenter, U. G. Froster-Iskenius, J.-P. Fryns, T. W. Glover, K.-H. Gustavson, S. F. Hoegerman, G. Holmgren, P. N. Howard-Peebles, E. C. Jenkins, M. S. Krawczun, G. Neri, A. Pettigrew, T. Schaap, S. A. Schonberg, L. R. Shapiro, N. Spinner, P. Steinbach, A. M. Vianna-Morgante, M. S. Watson and P. L. Wilmot

      Article first published online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320380249

    2. Genetic and other factors that contribute to variability in cytogenetic expression in fragile X males (pages 404–407)

      Gene S. Fisch, Wayne Silverman and Edmund C. Jenkins

      Article first published online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320380250

    3. Cytogenetic diagnosis of the fragile X syndrome: Efficiency, utilization, and trends (pages 408–410)

      Lawrence R. Shapiro, Patrick L. Wilmot, Deborah A. Shapiro, Isabel M. Pettersen and Anthony C. Casamassima

      Article first published online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320380251

    4. X chromosome inactivation in fibroblasts of mentally retarded female carriers of the fragile site Xq27.3: Application of the probe M27β to evaluate X inactivation status (pages 411–415)

      Dr. Malgorzata Schmidt, Desirée Du Sart, Paul Kalitsis, Neil Fraser, Margaret Leversha, Lucille Voullaire, Dean Foster, Julie Davies, Louise Hills, Vida Petrovic and Rhonda Hutchinson

      Article first published online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320380252

    5. Transformation and establishment of fragile X cell lines from amniocytes (pages 416–417)

      Lauren S. Jenkins, Dieter C. Gruenert, Edmund C. Jenkins and Steven A. Schonberg

      Article first published online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320380253

    6. New somatic cell hybrids for physical mapping in distal Xq and the fragile X region (pages 418–420)

      Susan A. Ledbetter, Charles E. Schwartz, Kay E. Davies and Dr. David H. Ledbetter

      Article first published online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320380254

    7. Effect of X inactivation on fragile X frequency and mental retardation (pages 421–424)

      Carla Rosenberg, Angela M. Vianna-Morgante, Paulo A. Otto and Leda Navajas

      Article first published online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320380255

    8. Endoreduplication and polyploidy in fragile X cells induced by methotrexate and fluorodeoxyuridine: Implications for diagnosis (pages 429–433)

      C. Kimchi-Sarfaty, R. Goitein, B. Kerem, M. Werner, B. Meidan and T. Schaap

      Article first published online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320380257

    9. Distribution of diploidy, polyploidy, and endoreduplication in fra(X) positive and negative lymphocytes, amniocytes, and chorionic Villi (pages 434–436)

      Edmund C. Jenkins, Maureen M. Sanz, James H. Ray, Sandra L. Stark-Houck and W. Ted Brown

      Article first published online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320380258

    10. Autosomal folate sensitive fragile sites in normal and mentally retarded individuals in Greece (pages 437–439)

      Ariadni Mavrou, Maria Syrrou, Christine Tsenghi and Catherine Metaxotou

      Article first published online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320380259

    11. Origin of the supernumerary X chromosome in a patient with fragile X and Klinefelter syndrome (pages 440–444)

      Dr. Kenneth G. Kupke, A. Lee Soreng and Ulrich Müller

      Article first published online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320380260

  13. Letter to the Editor

    1. Top of page
    2. Masthead
    3. Introduction
    4. Nosology
    5. Letter to the Editor
    6. Nosology
    7. Letter to the Editor
    8. Clinical Anthropometry
    9. Letter to the Editor
    10. Linkage, Carrier, Molecular, and Genetic Studies
    11. Letter to the Editor
    12. Linkage, Carrier, Molecular, and Genetic Studies
    13. Cytogenetics and Somatic Cell Genetics
    14. Letter to the Editor
    15. Prenatal Diagnosis
    16. Psychology, Neurology, and Neuropathology
    17. Letter to the Editor
    18. Psychology, Neurology, and Neuropathology
    19. Abstracts
    1. Fragile X expression: Use of a double induction system (pages 445–446)

      Dr. Patricia N. Howard-Peebles

      Article first published online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320380261

  14. Prenatal Diagnosis

    1. Top of page
    2. Masthead
    3. Introduction
    4. Nosology
    5. Letter to the Editor
    6. Nosology
    7. Letter to the Editor
    8. Clinical Anthropometry
    9. Letter to the Editor
    10. Linkage, Carrier, Molecular, and Genetic Studies
    11. Letter to the Editor
    12. Linkage, Carrier, Molecular, and Genetic Studies
    13. Cytogenetics and Somatic Cell Genetics
    14. Letter to the Editor
    15. Prenatal Diagnosis
    16. Psychology, Neurology, and Neuropathology
    17. Letter to the Editor
    18. Psychology, Neurology, and Neuropathology
    19. Abstracts
    1. Improved prenatal detection of fra(X)(q27.3): Methods for prevention of false negatives in chorionic villus and amniotic fluid cell cultures (pages 447–452)

      Edmund C. Jenkins, Michael S. Krawczun, Sandra L. Stark-Houck, Charlotte J. Duncan, Suphat Kunaporn, Hong Gu, Carol Schwartz-Richstein, Patricia N. Howard-Peebles, Anne Gross, Stephanie L. Sherman and W. Ted Brown

      Article first published online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320380262

    2. Prenatal diagnosis of the fragile X syndrome: Possible end of the experimental phase for amniotic fluid (pages 453–455)

      Lawrence R. Shapiro, Patrick L. Wilmot and Patricia D. Murphy

      Article first published online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320380263

    3. Distribution of autosomal fragile sites in specimens cultured for prenatal fragile X diagnosis (pages 456–463)

      Michael S. Krawczun, Edmund C. Jenkins, Charlotte J. Duncan, Sandra L. Stark-Houck, Suphat Kunaporn, Carol Schwartz-Richstein, Hong Gu and W. Ted Brown

      Article first published online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320380264

    4. SV40-transformed fragile (X) amniocytes (pages 464–466)

      Edmund C. Jenkins, Steven E. Brooks, Sandra L. Stark-Houck, Charlotte J. Duncan, Susan L. Sklower Brooks and W. Ted Brown

      Article first published online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320380265

  15. Psychology, Neurology, and Neuropathology

    1. Top of page
    2. Masthead
    3. Introduction
    4. Nosology
    5. Letter to the Editor
    6. Nosology
    7. Letter to the Editor
    8. Clinical Anthropometry
    9. Letter to the Editor
    10. Linkage, Carrier, Molecular, and Genetic Studies
    11. Letter to the Editor
    12. Linkage, Carrier, Molecular, and Genetic Studies
    13. Cytogenetics and Somatic Cell Genetics
    14. Letter to the Editor
    15. Prenatal Diagnosis
    16. Psychology, Neurology, and Neuropathology
    17. Letter to the Editor
    18. Psychology, Neurology, and Neuropathology
    19. Abstracts
    1. The fra(X) syndrome: Neurological, electrophysiological, and neuropathological abnormalities (pages 476–480)

      K. E. Wisniewski, S. M. Segan, C. M. Miezejeski, E. A. Sersen and R. D. Rudelli

      Article first published online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320380267

    2. Relationship between age and IQ among fragile X males: A multicenter study (pages 481–487)

      Gene S. Fisch, Tadao Arinami, Ursula Froster-Iskenius, Jean-Pierre Fryns, L. M. Curfs, M. Borghgraef, Patricia N. Howard-Peebles, Charles E. Schwartz, Richard J. Simensen and Lawrence R. Shapiro

      Article first published online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320380268

    3. Short-term memory and cognitive variability in adult fragile X females (pages 488–492)

      Dr. Robert de von Flindt, Bohdan Bybel, Albert E. Chudley and Fatima Lopes

      Article first published online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320380269

    4. Syntactic delay and pragmatic deviance in the language of fragile X males (pages 493–497)

      Vicki Sudhalter, Hollis S. Scarborough and Ira L. Cohen

      Article first published online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320380270

    5. Effects of age and communication level on eye contact in fragile X males and non-fragile X autistic males (pages 498–502)

      Ira L. Cohen, Peter M. Vietze, Vicki Sudhalter, Edmund C. Jenkins and W. Ted Brown

      Article first published online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320380271

    6. Mental impairment in cytogenetically positive fragile X females (pages 503–504)

      Amy Cronister, Randi J. Hagerman, Michael Wittenberger and Khaled Amiri

      Article first published online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320380272

    7. Cognitive profiles of the carrier fragile X woman (pages 505–508)

      Sharon S. Brainard, Rebecca A. Schreiner and Randi J. Hagerman MD

      Article first published online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320380273

  16. Letter to the Editor

    1. Top of page
    2. Masthead
    3. Introduction
    4. Nosology
    5. Letter to the Editor
    6. Nosology
    7. Letter to the Editor
    8. Clinical Anthropometry
    9. Letter to the Editor
    10. Linkage, Carrier, Molecular, and Genetic Studies
    11. Letter to the Editor
    12. Linkage, Carrier, Molecular, and Genetic Studies
    13. Cytogenetics and Somatic Cell Genetics
    14. Letter to the Editor
    15. Prenatal Diagnosis
    16. Psychology, Neurology, and Neuropathology
    17. Letter to the Editor
    18. Psychology, Neurology, and Neuropathology
    19. Abstracts
    1. Seizure disorders in the fragile X chromosome Syndrome (page 509)

      Frederick Hecht

      Article first published online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320380274

    2. Epileptic seizures and fra(X) syndrome (page 510)

      Paolo Bergonzi, Raffaele Ferri, Maurizio Elia and Sebastiano A. Musumeci

      Article first published online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320380275

  17. Psychology, Neurology, and Neuropathology

    1. Top of page
    2. Masthead
    3. Introduction
    4. Nosology
    5. Letter to the Editor
    6. Nosology
    7. Letter to the Editor
    8. Clinical Anthropometry
    9. Letter to the Editor
    10. Linkage, Carrier, Molecular, and Genetic Studies
    11. Letter to the Editor
    12. Linkage, Carrier, Molecular, and Genetic Studies
    13. Cytogenetics and Somatic Cell Genetics
    14. Letter to the Editor
    15. Prenatal Diagnosis
    16. Psychology, Neurology, and Neuropathology
    17. Letter to the Editor
    18. Psychology, Neurology, and Neuropathology
    19. Abstracts
    1. Epilepsy and fragile X syndrome: A follow-up study (pages 511–513)

      Dr. S. A. Musumeci, R. Ferri, M. Elia, R. M. Colognola, P. Bergonzi and C. A. Tassinari

      Article first published online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320380276

  18. Abstracts

    1. Top of page
    2. Masthead
    3. Introduction
    4. Nosology
    5. Letter to the Editor
    6. Nosology
    7. Letter to the Editor
    8. Clinical Anthropometry
    9. Letter to the Editor
    10. Linkage, Carrier, Molecular, and Genetic Studies
    11. Letter to the Editor
    12. Linkage, Carrier, Molecular, and Genetic Studies
    13. Cytogenetics and Somatic Cell Genetics
    14. Letter to the Editor
    15. Prenatal Diagnosis
    16. Psychology, Neurology, and Neuropathology
    17. Letter to the Editor
    18. Psychology, Neurology, and Neuropathology
    19. Abstracts
    1. Abstracts (pages 514–516)

      Article first published online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320380277

SEARCH

SEARCH BY CITATION