American Journal of Medical Genetics

Cover image for American Journal of Medical Genetics

May - June 1988

Volume 30, Issue 1-2

Pages fmi–fmi, 1–702

Currently known as: American Journal of Medical Genetics Part A

  1. Masthead

    1. Top of page
    2. Masthead
    3. Articles
    4. Clinical Studies and Nosology
    5. Letter to the Editors
    6. Clinical Studies and Nosology
    7. Addendum
    8. Clinical Studies and Nosology
    9. Prenatal Diagnosis and Treatments
    10. Cytogenetics
    11. Letter to the Editors
    12. Mapping and Linkages
    13. Molecular Basis
    14. Genetics and Epidemiology
    15. Hypotheses
    1. Masthead (page fmi)

      Article first published online: 8 JUN 2005 | DOI: 10.1002/ajmg.1320300101

  2. Articles

    1. Top of page
    2. Masthead
    3. Articles
    4. Clinical Studies and Nosology
    5. Letter to the Editors
    6. Clinical Studies and Nosology
    7. Addendum
    8. Clinical Studies and Nosology
    9. Prenatal Diagnosis and Treatments
    10. Cytogenetics
    11. Letter to the Editors
    12. Mapping and Linkages
    13. Molecular Basis
    14. Genetics and Epidemiology
    15. Hypotheses
    1. Conference report: Third International Workshop on the fragile X and X-linked mental retardation (pages 1–29)

      Giovanni Neri, John M. Opitz, Margareta Mikkelsen, Patricia A. Jacobs, Kay Davies and Gillian Turner

      Article first published online: 8 JUN 2005 | DOI: 10.1002/ajmg.1320300102

  3. Clinical Studies and Nosology

    1. Top of page
    2. Masthead
    3. Articles
    4. Clinical Studies and Nosology
    5. Letter to the Editors
    6. Clinical Studies and Nosology
    7. Addendum
    8. Clinical Studies and Nosology
    9. Prenatal Diagnosis and Treatments
    10. Cytogenetics
    11. Letter to the Editors
    12. Mapping and Linkages
    13. Molecular Basis
    14. Genetics and Epidemiology
    15. Hypotheses
    1. Suggestively increased rate of infant death in children of fra(X) positive mothers (pages 73–75)

      Jean-Pierre Fryns, Philippe Moerman, Filip Gilis, Luc d'Espallier and Herman Van Den Berghe

      Article first published online: 8 JUN 2005 | DOI: 10.1002/ajmg.1320300105

    2. Fragile X syndrome and neoplasia (pages 77–82)

      Dr. Mary C. Phelan, Roger E. Stevenson, Jack L. Collins and Howard E. Trent III

      Article first published online: 8 JUN 2005 | DOI: 10.1002/ajmg.1320300106

    3. Aortic hypoplasia and cardiac valvular abnormalities in a boy with fragile X syndrome (pages 83–98)

      Gail Waldstein and Randi Hagerman

      Article first published online: 8 JUN 2005 | DOI: 10.1002/ajmg.1320300107

    4. Fragile-X mutation and Klinefelter syndrome: A reappraisal (pages 99–107)

      Filippi G., Pecile V., Rinaldi A. and Siniscalco M.

      Article first published online: 8 JUN 2005 | DOI: 10.1002/ajmg.1320300108

    5. The concurrence of Klinefelter syndrome and fragile X syndrome (pages 109–113)

      Jean-Pierre Fryns and Herman Van Den Berghe

      Article first published online: 8 JUN 2005 | DOI: 10.1002/ajmg.1320300109

    6. Aneuploidy and the fragile X syndrome (pages 115–121)

      Michael S. Watson, W. Roy Breg, David Pauls, W. Ted Brown, Andrew J. Carroll, Patricia N. Howard-Peebles, David Meryash and Lawrence R. Shapiro

      Article first published online: 8 JUN 2005 | DOI: 10.1002/ajmg.1320300110

    7. Fragile X syndrome: Growth, development, and intellectual function (pages 123–142)

      Leonard A. Prouty, R. Curtis Rogers, Roger E. Stevenson, Jane H. Dean, Kim K. Palmer, Richard J. Simensen, Gale N. Coston and Charles E. Schwartz

      Article first published online: 8 JUN 2005 | DOI: 10.1002/ajmg.1320300111

    8. Growth pattern in boys with fragile X (pages 143–147)

      Karen Brøndum Nielsen

      Article first published online: 8 JUN 2005 | DOI: 10.1002/ajmg.1320300112

    9. Anthropometry in Martin-Bell syndrome (pages 149–164)

      Dr. Danuta Z. Loesch, Maureen Lafranchi and David Scott

      Article first published online: 8 JUN 2005 | DOI: 10.1002/ajmg.1320300113

    10. Preliminary communication: Photoanthropometric analysis of individuals with the fragile X syndrome (pages 165–168)

      Merlin G. Butler, G. Andy Allen, Dharmdeo N. Singh, Nancy J. Carpenter and Bryan D. Hall

      Article first published online: 8 JUN 2005 | DOI: 10.1002/ajmg.1320300114

    11. The predictive value of dermatoglyphic anomalies in the diagnosis of fra(X)-positive Martin-Bell syndrome (MBS) (pages 169–175)

      Ulrich Langenbeck, Isabell Varga and Ingo Hansmann

      Article first published online: 8 JUN 2005 | DOI: 10.1002/ajmg.1320300115

    12. A dermatoglyphic study of a group of Sicilian children with fragile-X syndrome (pages 177–183)

      G. Milone, L. Conti, R. Rizzo, S. Sanfilippo, V. Sammito and C. Romano

      Article first published online: 8 JUN 2005 | DOI: 10.1002/ajmg.1320300116

    13. Crown size asymmetry in males with fra (X) or Martin-Bell syndrome (pages 185–190)

      B. Peretz, P. Ever-Hadani, P. Casamassimo, E. Eidelman, C. Shellhart and R. Hagerman

      Article first published online: 8 JUN 2005 | DOI: 10.1002/ajmg.1320300117

    14. Cognitive profiles of boys with the fragile X syndrome (pages 191–200)

      Melinda B. Kemper, Dr. Randi J. Hagerman and Debra Altshul-Stark

      Article first published online: 8 JUN 2005 | DOI: 10.1002/ajmg.1320300118

    15. Fragile X syndrome: Neuropathology center (pages 201–205)

      W. Ted Brown, Raul D. Rudelli and Henry M. Wisniewski

      Article first published online: 8 JUN 2005 | DOI: 10.1002/ajmg.1320300119

    16. Prevalence of a novel epileptogenic EEG pattern in the Martin-Bell syndrome (pages 207–212)

      S. A. Musumeci, R. Ferri, R. M. Colognola, G. Neri, S. Sanfilippo and P. Bergonzi

      Article first published online: 8 JUN 2005 | DOI: 10.1002/ajmg.1320300120

    17. Variable expression of the fragile X syndrome in heterozygous females of normal intelligence (pages 213–225)

      Peter H. Wolff, Judith Gardner, John Lappen, Jeanne Paccia and David Meryash

      Article first published online: 8 JUN 2005 | DOI: 10.1002/ajmg.1320300121

    18. The fragile X syndrome: Variability of expression in carrier females (pages 227–230)

      Dr. Patricia N. Howard-Peebles and W. Ted Brown

      Article first published online: 8 JUN 2005 | DOI: 10.1002/ajmg.1320300122

    19. Case report: Fragile X syndrome and nephrogenic diabetes insipidus (pages 231–236)

      Dr. G. K. Suthers, G. Turner and J. C. Mulley

      Article first published online: 8 JUN 2005 | DOI: 10.1002/ajmg.1320300123

  4. Letter to the Editors

    1. Top of page
    2. Masthead
    3. Articles
    4. Clinical Studies and Nosology
    5. Letter to the Editors
    6. Clinical Studies and Nosology
    7. Addendum
    8. Clinical Studies and Nosology
    9. Prenatal Diagnosis and Treatments
    10. Cytogenetics
    11. Letter to the Editors
    12. Mapping and Linkages
    13. Molecular Basis
    14. Genetics and Epidemiology
    15. Hypotheses
    1. Autism and the fragile X syndrome (pages 237–238)

      Dr. Stewart L. Einfeld

      Article first published online: 8 JUN 2005 | DOI: 10.1002/ajmg.1320300124

  5. Clinical Studies and Nosology

    1. Top of page
    2. Masthead
    3. Articles
    4. Clinical Studies and Nosology
    5. Letter to the Editors
    6. Clinical Studies and Nosology
    7. Addendum
    8. Clinical Studies and Nosology
    9. Prenatal Diagnosis and Treatments
    10. Cytogenetics
    11. Letter to the Editors
    12. Mapping and Linkages
    13. Molecular Basis
    14. Genetics and Epidemiology
    15. Hypotheses
    1. A new syndrome with mental retardation, short stature and an Xq duplication (pages 239–250)

      Dr. A. Thode, M. W. Partington, M-Y Yip, C. Chapman, V. F. Richardson and G. Turner

      Article first published online: 8 JUN 2005 | DOI: 10.1002/ajmg.1320300125

  6. Addendum

    1. Top of page
    2. Masthead
    3. Articles
    4. Clinical Studies and Nosology
    5. Letter to the Editors
    6. Clinical Studies and Nosology
    7. Addendum
    8. Clinical Studies and Nosology
    9. Prenatal Diagnosis and Treatments
    10. Cytogenetics
    11. Letter to the Editors
    12. Mapping and Linkages
    13. Molecular Basis
    14. Genetics and Epidemiology
    15. Hypotheses
    1. You have free access to this content
      Addendum (page 250)

      Article first published online: 8 JUN 2005 | DOI: 10.1002/ajmg.1320300126

  7. Clinical Studies and Nosology

    1. Top of page
    2. Masthead
    3. Articles
    4. Clinical Studies and Nosology
    5. Letter to the Editors
    6. Clinical Studies and Nosology
    7. Addendum
    8. Clinical Studies and Nosology
    9. Prenatal Diagnosis and Treatments
    10. Cytogenetics
    11. Letter to the Editors
    12. Mapping and Linkages
    13. Molecular Basis
    14. Genetics and Epidemiology
    15. Hypotheses
    1. X-linked mental retardation with dystonic movements of the hands (pages 251–262)

      M. W. Partington, J. C. Mulley, G. R. Sutherland, A. Hockey, A. Thode and G. Turner

      Article first published online: 8 JUN 2005 | DOI: 10.1002/ajmg.1320300127

    2. X-linked mental retardation associated with psoriasis: A new syndrome? (pages 263–273)

      Lisbeth Tranebjærg, Arne Svejgaard and Gert Lykkesfeldt

      Article first published online: 8 JUN 2005 | DOI: 10.1002/ajmg.1320300128

    3. Simpson-Golabi-Behmel syndrome: An X-linked encephalo-trophoschisis syndrome (pages 287–299)

      Prof. G. Neri, R. Marini, M. Cappa, P. Borrelli and J. M. Opitz

      Article first published online: 8 JUN 2005 | DOI: 10.1002/ajmg.1320300130

    4. Simpson-Golabi-Behmel syndrome: Follow-up of the michigan family (pages 301–308)

      John M. Opitz, Jürgen Herrmann, Enid F. Gilbert and Reuben Matalon

      Article first published online: 8 JUN 2005 | DOI: 10.1002/ajmg.1320300131

    5. FG syndrome update 1988: Note of 5 new patients and bibliography (pages 309–328)

      John M. Opitz, Antonio Richieri-Da Costa, Jon M. Aase and Paul J. Benke

      Article first published online: 8 JUN 2005 | DOI: 10.1002/ajmg.1320300132

  8. Prenatal Diagnosis and Treatments

    1. Top of page
    2. Masthead
    3. Articles
    4. Clinical Studies and Nosology
    5. Letter to the Editors
    6. Clinical Studies and Nosology
    7. Addendum
    8. Clinical Studies and Nosology
    9. Prenatal Diagnosis and Treatments
    10. Cytogenetics
    11. Letter to the Editors
    12. Mapping and Linkages
    13. Molecular Basis
    14. Genetics and Epidemiology
    15. Hypotheses
    1. Recent experience in prenatal fra(X) detection (pages 329–336)

      Edmund C. Jenkins, W. Ted Brown, Michael S. Krawczun, Charlotte J. Duncan, Kusum P. Lele, Eduardo S. Cantu, Steven Schonberg, Mitchell S. Golbus, Gurbax S. Sekhon, Sandra Stark, Suphat Kunaporn and Wayne P. Silverman

      Article first published online: 8 JUN 2005 | DOI: 10.1002/ajmg.1320300133

    2. Prenatal diagnosis of the fragile X – The Australasian experience (pages 337–345)

      Stuart G. Purvis-Smith, Sue Laing, Grant R. Sutherland and Elizabeth Baker

      Article first published online: 8 JUN 2005 | DOI: 10.1002/ajmg.1320300134

    3. Prenatal diagnosis of fragile X syndrome by placental (chorionic villi) biopsy culture (pages 355–368)

      Mark J. McKinley, Lyndal U. Kearney, Kypros H. Nicolaides, Christine M. Gosden, Tessa P. Webb and Jean P. Fryns

      Article first published online: 8 JUN 2005 | DOI: 10.1002/ajmg.1320300136

    4. Fragile X expression in normal and mentally retarded subjects: Effect of treatment with an antifolic agent (pages 369–376)

      S. Sanfilippo, R. M. Ragusa, F. Scillato, M. Ruggeri and Prof. G. Neri

      Article first published online: 8 JUN 2005 | DOI: 10.1002/ajmg.1320300137

    5. A controlled trial of stimulant medication in children with the fragile X syndrome (pages 377–392)

      Randi J. Hagerman, Mary A. Murphy and Michael D. Wittenberger

      Article first published online: 8 JUN 2005 | DOI: 10.1002/ajmg.1320300138

    6. Folic acid treatment of fragile X males: A further study (pages 393–399)

      Gene S. Fisch, Ira L. Cohen, Anne C. Gross, Valerie Jenkins, Edmund C. Jenkins and W. T. Brown

      Article first published online: 8 JUN 2005 | DOI: 10.1002/ajmg.1320300139

  9. Cytogenetics

    1. Top of page
    2. Masthead
    3. Articles
    4. Clinical Studies and Nosology
    5. Letter to the Editors
    6. Clinical Studies and Nosology
    7. Addendum
    8. Clinical Studies and Nosology
    9. Prenatal Diagnosis and Treatments
    10. Cytogenetics
    11. Letter to the Editors
    12. Mapping and Linkages
    13. Molecular Basis
    14. Genetics and Epidemiology
    15. Hypotheses
    1. Inactivation pattern of the fragile X in heterozygous carriers (pages 401–406)

      Jean-Pierre Fryns and Herman Van Den Berghe

      Article first published online: 8 JUN 2005 | DOI: 10.1002/ajmg.1320300140

    2. Fra(X) frequency on the active X-chromosome and phenotype in heterozygous carriers of the fra(X) form of mental retardation (pages 407–415)

      Dorothea Wilhelm, Ursula Froster-Iskenius, Jürgen Paul and Eberhard Schwinger

      Article first published online: 8 JUN 2005 | DOI: 10.1002/ajmg.1320300141

    3. Screening for the fragile X: How many cells should we analyse? (pages 417–422)

      Niels Tommerup, Susan Laing, Ib Jarle Christensen and Gillian Turner

      Article first published online: 8 JUN 2005 | DOI: 10.1002/ajmg.1320300142

    4. Fragile (X) expression, age and the degree of intellectual handicap in the male (pages 423–428)

      Dr. Gillian Turner and Michael W. Partington

      Article first published online: 8 JUN 2005 | DOI: 10.1002/ajmg.1320300143

    5. Constitutive fragile sites in fra(X) individuals (pages 429–434)

      Edmund C. Jenkins, Kusum P. Lele, Michael S. Krawczun, Anne C. Gross, Charlotte J. Duncan and W. Ted Brown

      Article first published online: 8 JUN 2005 | DOI: 10.1002/ajmg.1320300144

    6. Fragile X expression in short-term whole blood cultures is affected by cell density (pages 435–442)

      Dr. Michael S. Krawczun, Edmund C. Jenkins, W. Ted Brown and Wayne P. Silverman

      Article first published online: 8 JUN 2005 | DOI: 10.1002/ajmg.1320300145

    7. In situ nick translation of the fragile X region (pages 443–450)

      Sarah L. Nolin, Edmund C. Jenkins, W. Ted Brown and Carl S. Dobkin

      Article first published online: 8 JUN 2005 | DOI: 10.1002/ajmg.1320300146

  10. Letter to the Editors

    1. Top of page
    2. Masthead
    3. Articles
    4. Clinical Studies and Nosology
    5. Letter to the Editors
    6. Clinical Studies and Nosology
    7. Addendum
    8. Clinical Studies and Nosology
    9. Prenatal Diagnosis and Treatments
    10. Cytogenetics
    11. Letter to the Editors
    12. Mapping and Linkages
    13. Molecular Basis
    14. Genetics and Epidemiology
    15. Hypotheses
    1. Fragile X testing in mothers of transmitting males (pages 455–457)

      Patricia Howard-Peebles and Ursula Froster-Iskenius

      Article first published online: 8 JUN 2005 | DOI: 10.1002/ajmg.1320300148

  11. Mapping and Linkages

    1. Top of page
    2. Masthead
    3. Articles
    4. Clinical Studies and Nosology
    5. Letter to the Editors
    6. Clinical Studies and Nosology
    7. Addendum
    8. Clinical Studies and Nosology
    9. Prenatal Diagnosis and Treatments
    10. Cytogenetics
    11. Letter to the Editors
    12. Mapping and Linkages
    13. Molecular Basis
    14. Genetics and Epidemiology
    15. Hypotheses
    1. Is there a fragile(X) negative Martin-Bell syndrome? (pages 459–471)

      Dr. A. Thode, S. Laing, M. W. Partington and G. Turner

      Article first published online: 8 JUN 2005 | DOI: 10.1002/ajmg.1320300149

    2. Linkage analysis suggests at least two loci for X-linked nonspecific mental retardation (pages 473–483)

      B. Arveiler, Y. Alembik, A. Hanauer, P. Jacobs, L. Tranebjaerg, M. Mikkelsen, H. Puissant, L. Larget Piet and J. L. Mandel

      Article first published online: 8 JUN 2005 | DOI: 10.1002/ajmg.1320300150

    3. A non-syndromal form of X-linked mental retardation (XLMR) is linked to DXS14 (pages 485–491)

      Dr. G. K. Suthers, G. Turner and J. C. Mulley

      Article first published online: 8 JUN 2005 | DOI: 10.1002/ajmg.1320300151

    4. Linkage studies with the gene for an X-linked syndrome of mental retardation, microcephaly and spastic diplegia (MRX2) (pages 493–508)

      Dr. G. R. Sutherland, A. K. Gedeon, E. A. Haan, P. Woodroffe and J. C. Mulley

      Article first published online: 8 JUN 2005 | DOI: 10.1002/ajmg.1320300152

    5. A family with the Coffin Lowry syndrome revisited: Localization of CLS to Xp21-pter (pages 509–521)

      Dr. M. W. Partington, J. C. Mulley, G. R. Sutherland, A. Thode and G. Turner

      Article first published online: 8 JUN 2005 | DOI: 10.1002/ajmg.1320300153

    6. Probable localisation of the Coffin-Lowry locus in Xp22.2-P22.1 by multipoint linkage analysis (pages 523–530)

      A. Hanauer, Y. Alembik, S. Gilgenkrantz, P. Mujica, A. Nivelon-Chevallier, M. E. Pembrey, I. D. Young and J. L. Mandel

      Article first published online: 8 JUN 2005 | DOI: 10.1002/ajmg.1320300154

    7. Fragile X syndrome: Linkage analysis in black and white populations (pages 531–542)

      Dr. C. E. Schwartz, M. C. Phelan, C. Brightharp, I. Pancoast, P. N. Howard-Peebles, S. Thibodeau, W. T. Brown and E. C. Jenkins

      Article first published online: 8 JUN 2005 | DOI: 10.1002/ajmg.1320300155

  12. Molecular Basis

    1. Top of page
    2. Masthead
    3. Articles
    4. Clinical Studies and Nosology
    5. Letter to the Editors
    6. Clinical Studies and Nosology
    7. Addendum
    8. Clinical Studies and Nosology
    9. Prenatal Diagnosis and Treatments
    10. Cytogenetics
    11. Letter to the Editors
    12. Mapping and Linkages
    13. Molecular Basis
    14. Genetics and Epidemiology
    15. Hypotheses
    1. Improved DNA markers for efficient analysis of fragile X families (pages 543–550)

      R. Heilig, I. Oberlé, B. Arveiler, A. Hanauer, M. Vidaud and J. L. Mandel

      Article first published online: 8 JUN 2005 | DOI: 10.1002/ajmg.1320300156

    2. Multipoint linkage of 9 anonymous probes to HPRT, factor 9, and fragile X (pages 551–566)

      W. Ted Brown, Wu Ye, Anne C. Gross, Colin B. Chan, Carl S. Dobkin and Edmund C. Jenkins

      Article first published online: 8 JUN 2005 | DOI: 10.1002/ajmg.1320300157

    3. Linkage between the fragile X and F9, DXS52 (St14), DXS98 (4D-8) and DXS105 (CX55.7) (pages 567–580)

      John Mulley, Gillian Turner, Sharon Bain and Grant R. Sutherland

      Article first published online: 8 JUN 2005 | DOI: 10.1002/ajmg.1320300158

    4. Pulsed-field gel mapping studies in the vicinity of the fragile site at Xq27.3 (pages 581–591)

      M. Patterson, M. Bell, C. Schwartz and Dr. K. Davies

      Article first published online: 8 JUN 2005 | DOI: 10.1002/ajmg.1320300159

    5. Pulsed-field gradient-gel studies around the fragile site (pages 593–600)

      Carl S. Dobkin and W. Ted Brown

      Article first published online: 8 JUN 2005 | DOI: 10.1002/ajmg.1320300160

    6. Cytogenetic and physical mapping in the region of the X chromosome surrounding the fragile site (pages 601–611)

      Catherine Nguyen, Marie-Geneviève Mattei, Juan Antonio Rey, Marie-Antoinette Baeteman, Jean-François Mattei and Bertrand R. Jordan

      Article first published online: 8 JUN 2005 | DOI: 10.1002/ajmg.1320300161

    7. Strategy for molecular cloning of the fragile X site DNA (pages 613–623)

      Stephen T. Warren, Fuping Zhang, James S. Sutcliffe and Jeanne F. Peters

      Article first published online: 8 JUN 2005 | DOI: 10.1002/ajmg.1320300162

  13. Genetics and Epidemiology

    1. Top of page
    2. Masthead
    3. Articles
    4. Clinical Studies and Nosology
    5. Letter to the Editors
    6. Clinical Studies and Nosology
    7. Addendum
    8. Clinical Studies and Nosology
    9. Prenatal Diagnosis and Treatments
    10. Cytogenetics
    11. Letter to the Editors
    12. Mapping and Linkages
    13. Molecular Basis
    14. Genetics and Epidemiology
    15. Hypotheses
    1. Investigation of the twinning rate in families with the fragile X syndrome (pages 625–631)

      S. L. Sherman, G. Turner, L. Sheffield, S. Laing and H. Robinson

      Article first published online: 8 JUN 2005 | DOI: 10.1002/ajmg.1320300163

    2. Investigation of the segregation of the fragile X mutation in daughters of obligate carrier women (pages 633–639)

      S. L. Sherman, G. Turner, H. Robinson and S. Laing

      Article first published online: 8 JUN 2005 | DOI: 10.1002/ajmg.1320300164

    3. Fragile X syndrome: Incidence, clinical and cytogenetic findings in the black and white populations of South Carolina (pages 641–654)

      Dr. C. E. Schwartz, M. C. Phelan, L. H. Pulliam, G. Wilkes, L. V. Vanner, K. L. Albiez, W. A. Potts, R. C. Rogers, R. J. Schroer, R. A. Saul, L. A. Prouty, J. H. Dean, H. A. Taylor and R. E. Stevenson

      Article first published online: 8 JUN 2005 | DOI: 10.1002/ajmg.1320300165

    4. Screening developmentally disabled male populations for fragile X: The effect of sample size (pages 655–663)

      Gene S. Fisch, Ira L. Cohen, Edmund C. Jenkins and W. T. Brown

      Article first published online: 8 JUN 2005 | DOI: 10.1002/ajmg.1320300166

    5. The fragile X in sicily: An epidemiological survey (pages 665–672)

      Prof. G. Neri, S. Sanfilippo, L. Pavone, F. Mollica, I. Barberi, L. Giuffre, C. Romano, T. Mattina, M. Cammarata, M. G. Ragusa, V. Sammito, G. Ventimiglia and S. A. Musumeci

      Article first published online: 8 JUN 2005 | DOI: 10.1002/ajmg.1320300167

    6. Fragile X families in a Northern Swedish county - a genealogical study demonstrating apparent paternal transmission from the 18th century (pages 673–679)

      Gösta Holmgren, Hans K. Son Blomquist, Ulf Drugge and Karl-Henrik Gustavson

      Article first published online: 8 JUN 2005 | DOI: 10.1002/ajmg.1320300168

  14. Hypotheses

    1. Top of page
    2. Masthead
    3. Articles
    4. Clinical Studies and Nosology
    5. Letter to the Editors
    6. Clinical Studies and Nosology
    7. Addendum
    8. Clinical Studies and Nosology
    9. Prenatal Diagnosis and Treatments
    10. Cytogenetics
    11. Letter to the Editors
    12. Mapping and Linkages
    13. Molecular Basis
    14. Genetics and Epidemiology
    15. Hypotheses
    1. Intercalary heterochromatin of Drosophila as a potential model for human fragile sites (pages 689–691)

      Charles D. Laird and Mary M. Lamb

      Article first published online: 8 JUN 2005 | DOI: 10.1002/ajmg.1320300170

    2. Fragile X expression in Martin-Bell syndrome, intellectually normal individuals, and neoplasia, interpreted by a viral hypothesis (pages 697–702)

      Fiorella Shabtai, Jacob Hart, Dvora Klar, Shlomo Bichacho and Isaac Halbrecht

      Article first published online: 8 JUN 2005 | DOI: 10.1002/ajmg.1320300172

SEARCH

SEARCH BY CITATION