American Journal of Medical Genetics

Cover image for American Journal of Medical Genetics

15 April - 1 May 1992

Volume 43, Issue 1-2

Pages fmi–fmi, 1–509

Currently known as: American Journal of Medical Genetics Part A

  1. Masthead

    1. Top of page
    2. Masthead
    3. Obituary
    4. Obituarys
    5. Conference Report
    6. Articles
    7. Invited Editorial Comment
    8. Articles
    9. Letter to the Editor
    10. Articles
    11. Letter To The Editors
    12. Articles
    13. Letter To The Editors
    14. Articles
    15. Brief Clinical Reports
    16. Articles
    1. You have free access to this content
      Masthead (page fmi)

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320430101

  2. Obituary

    1. Top of page
    2. Masthead
    3. Obituary
    4. Obituarys
    5. Conference Report
    6. Articles
    7. Invited Editorial Comment
    8. Articles
    9. Letter to the Editor
    10. Articles
    11. Letter To The Editors
    12. Articles
    13. Letter To The Editors
    14. Articles
    15. Brief Clinical Reports
    16. Articles
    1. In memoriam: Isabelle Oberlé (pages 1–2)

      Jean-Louis Mandel

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320430102

  3. Obituarys

    1. Top of page
    2. Masthead
    3. Obituary
    4. Obituarys
    5. Conference Report
    6. Articles
    7. Invited Editorial Comment
    8. Articles
    9. Letter to the Editor
    10. Articles
    11. Letter To The Editors
    12. Articles
    13. Letter To The Editors
    14. Articles
    15. Brief Clinical Reports
    16. Articles
    1. In memoriam: Michael S. Krawczun, Ph.D., D.A.B.M.G. [1952–1991] (pages 3–4)

      Dr. Edmund C. Jenkins

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320430103

  4. Conference Report

    1. Top of page
    2. Masthead
    3. Obituary
    4. Obituarys
    5. Conference Report
    6. Articles
    7. Invited Editorial Comment
    8. Articles
    9. Letter to the Editor
    10. Articles
    11. Letter To The Editors
    12. Articles
    13. Letter To The Editors
    14. Articles
    15. Brief Clinical Reports
    16. Articles
    1. Fifth international workshop on the fragile X and X-linked mental retardation (pages 5–27)

      Dr. Jean-Louis Mandel, Randi Hagerman, Ursula Froster, W. Ted Brown, Edmund C. Jenkins, Patricia Jacobs, Gillian Turner, Herbert Lubs and Giovanni Neri

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320430104

  5. Articles

    1. Top of page
    2. Masthead
    3. Obituary
    4. Obituarys
    5. Conference Report
    6. Articles
    7. Invited Editorial Comment
    8. Articles
    9. Letter to the Editor
    10. Articles
    11. Letter To The Editors
    12. Articles
    13. Letter To The Editors
    14. Articles
    15. Brief Clinical Reports
    16. Articles
    1. Longitudinal changes in IQ among fragile X males: Clinical evidence of more than one mutation? (pages 28–34)

      G. S. Fisch, L. R. Shapiro, R. Simensen, C. E. Schwartz, J. P. Fryns, M. Borghgraef, L. M. Curfs, P. N. Howard-Peebles, T. Arinami and A. Mavrou

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320430105

  6. Invited Editorial Comment

    1. Top of page
    2. Masthead
    3. Obituary
    4. Obituarys
    5. Conference Report
    6. Articles
    7. Invited Editorial Comment
    8. Articles
    9. Letter to the Editor
    10. Articles
    11. Letter To The Editors
    12. Articles
    13. Letter To The Editors
    14. Articles
    15. Brief Clinical Reports
    16. Articles
    1. Behavior phenotype of the fragile X syndrome (pages 56–60)

      Dr Stewart Enifeld and Wayne Hall

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320430108

  7. Articles

    1. Top of page
    2. Masthead
    3. Obituary
    4. Obituarys
    5. Conference Report
    6. Articles
    7. Invited Editorial Comment
    8. Articles
    9. Letter to the Editor
    10. Articles
    11. Letter To The Editors
    12. Articles
    13. Letter To The Editors
    14. Articles
    15. Brief Clinical Reports
    16. Articles
    1. Brief screening questionnaire for determining affected state in fragile X Syndrome: A consensus recommendation (pages 61–64)

      Allan L. Reiss, Carlo Cianchetti, Ira L. Cohen, Bert Devries, Randi Hagerman, Veronica Hinton, Ursula Froster, Ave Lachiewicz, Michele Mazzocco, William Sobesky and Vicki Sudhalter

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320430109

    2. Expressive semantic deficit in the productive language of males with fragile X syndrome (pages 65–71)

      Vicki Sudhalter, Maria Maranion and Patricia Brooks

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320430110

    3. Problem solving limitations among cytogenetically expressing fragile X women (pages 78–86)

      Michele M. M. Mazzocco, Randi J. Hagerman and Bruce F. Pennington

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320430112

    4. Mode of inheritance influences behavioral expression and molecular control of cognitive deficits in female carriers of the fragile X syndrome (pages 87–95)

      V. J. Hinton, C. S. Dobkin, J. M. Halperin, E. C. Jenkins, W. T. Brown, X. H. Ding, I. L. Cohen, F. Rousseau and C. M. Miezejeski

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320430113

    5. Prenatally detected fragile X females: Long-term follow-up studies show high risk of mental impairment (pages 96–102)

      W. Ted Brown, Edmund C. Jenkins, Ponmani Goonewardena, Charles Miezejeski, Joan Atkin and Didier Devys

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320430114

    6. Premutation for the martin-bell syndrome analyzed in a large sardinian family: II. Neuropsychological and behavioral data (pages 103–110)

      Carlo Cianchetti, Giorgio Filippi, Giuseppina Sannio-Fancello, Anna-Lisa Fratta, Maria-Giovanna Marrosu, Franca Dagna-Bricarell and Marcello Siniscalco

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320430115

    7. Verbal learning and memory among heterozygous fragile X females (pages 111–115)

      Jim Grigsby, Melinda B. Kemper and Randi J. Hagerman

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320430116

    8. Cognitive profile in adult, normal intelligent female fragile X carriers (pages 116–119)

      J. Steyaert, M. Borghgraef, C. Gaulthier, J. P. Fryns and H. Van Den Berghe

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320430117

    9. Mortality in the fragile X syndrome: Preliminary data (pages 120–123)

      M. W. Partington, H. Robinson, S. Laing and G. Turner

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320430118

    10. Sleep apnea in fragile X syndrome (pages 124–127)

      Emanuel Tirosh and Zvi Borochowitz

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320430119

    11. Prenatal detection of Fra(X)(q27.3) in female identical twins: Reliability of low level cytogenetic prenatal expression in females (pages 128–135)

      Edmund C. Jenkins, W. Ted Brown, Steven Schonberg, Michael S. Krawczun, James Goldberg and Mitchell S. Golbus

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320430120

    12. Fra(X)(q27.2), the common fragile site, observed in only one of 760 cases studied for the fragile X syndrome (pages 136–141)

      Edmund C. Jenkins, Marilyn J. Genovese, Charlotte J. Duncan, Hong Gu, Sandra L. Stark-Houck, Kusum Lele, Shu-Yun Li and Michael S. Krawczun

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320430121

    13. Fra(X) prenatal diagnosis: Are endoreduplicated and polyploid cells useful diagnostic criteria? (pages 149–154)

      Michael S. Krawczun, Charlotte J. Duncan, Sandra L. Stark-Houck and Edmund C. Jenkins

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320430123

    14. Dialyzed fetal Bovine serum increases cytogenetic fragile X expression (pages 155–160)

      Edmund C. Jenkins, Charlotte J. Duncan, Hong Gu, Marilyn Genovese and Michael S. Krawczun

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320430124

  8. Letter to the Editor

    1. Top of page
    2. Masthead
    3. Obituary
    4. Obituarys
    5. Conference Report
    6. Articles
    7. Invited Editorial Comment
    8. Articles
    9. Letter to the Editor
    10. Articles
    11. Letter To The Editors
    12. Articles
    13. Letter To The Editors
    14. Articles
    15. Brief Clinical Reports
    16. Articles
    1. Effect of dialyzed sera on fragile X expression (page 161)

      Patricia N. Howard-Peebles

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320430125

  9. Articles

    1. Top of page
    2. Masthead
    3. Obituary
    4. Obituarys
    5. Conference Report
    6. Articles
    7. Invited Editorial Comment
    8. Articles
    9. Letter to the Editor
    10. Articles
    11. Letter To The Editors
    12. Articles
    13. Letter To The Editors
    14. Articles
    15. Brief Clinical Reports
    16. Articles
    1. Recent experience in prenatal diagnosis of fragile X (pages 162–166)

      Dr. Patricia N. Howard-Peebles and Anne Maddalena

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320430126

    2. Prenatal cytogenetic diagnosis of the fragile X syndrome in amniotic fluid: Calculation of accuracy (pages 170–173)

      Lawrence R. Shapiro, Patrick L. Wilmot and Gene S. Fisch

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320430128

    3. Prenatal diagnosis and carrier detection in fragile X (pages 174–180)

      Harriet Von Koskull, Ann-Marie Nordström, Riitta Salonen and Leena Peltonen

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320430129

    4. Prenatal diagnosis of fragile X syndrome: Results from parallel molecular and cytogenetic studies (pages 181–186)

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

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320430130

    5. Limited size of the fragile X site shown by fluorescence in situ hybridization (pages 187–191)

      Annemieke J. M. H. Verkerk, Bert H. J. Eussen, Jan O. Van Hemel and Dr. Ben A. Oostra

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320430131

    6. Intragenic probe used for diagnostics in fragile X families (pages 192–196)

      Annemieke J. M. H. Verkerk, Bert B. A. De Vries, Martinus F. Niermeijer, Ying-Hui Fu, David L. Nelson, Stephen T. Warren, Danielle F. Majoor-Krakauer, Dicky J. J. Halley and Dr. Ben A. Oostra

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320430132

    7. On some technical aspects of direct DNA diagnosis of the fragile X syndrome (pages 197–207)

      F. Rousseau, D. Heitz, V. Biancalana, I. Oberlé and J. L. Mandel

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320430133

    8. Molecular studies of the fragile X syndrome (pages 217–223)

      Samantha J. L. Knight, Mark C. Hirst, Anya Roche, Zoe Christodoulou, Susan M. Huson, Robin Winter, Margaret Fitchett, Mark J. McKinley, Richard H. Lindenbaum, Yutaka Nakahori and Dr. Kay E. Davies

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320430135

    9. Three families with high expression of a fragile site at Xq27.3, lack of anomalies at the FMR-1 CpG Island, and no clear phenotypic association (pages 224–231)

      I. Oberlé, J. Boué, M. F. Croquette, M. A. Voelckel, M. G. Mattei and J. L. Mandel

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320430136

    10. Characterization of a highly polymorphic dinucleotide repeat 150 KB proximal to the fragile X site (pages 237–243)

      Gregory J. Riggins, Stephanie L. Sherman, Ben A. Oostra, James S. Sutcliffe, David Feitell, David L. Nelson, Bernard A. Van Oost, Arie P. T. Smits, Feliciano J. Ramos, Ellen Pfendner, Derek P. A. Kuhl, C. Thomas Caskey and Stephen T. Warren

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320430138

    11. Analysis of mutations at the fragile X locus using the DNA probe Ox1.9 (pages 244–254)

      Karen Snow, Laurie Doud, Randi Hagerman, Claire Hull, Mark C. Hirst, Kay E. Davies and Stephen L. Thibodeau

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320430139

    12. Parental origin of the Fra(X) gene is a major determinant of the cytogenetic expression and the CGG repeat length in female carriers (pages 261–267)

      Arie Smits, Dominique Smeets, Jos Dreesen, Ben Hamel, Anton de Haan and Bernard van Oost

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320430141

    13. Methylation and mutation patterns in the fragile X syndrome (pages 268–278)

      Helena Malmgren, Marie-Louise Steén-Bondeson, Karl-Henrik Gustavson, Eva Seémanova, Gösta Holmgren, Isabelle Oberlé, Jean-Louis Mandel, Ulf Pettersson and Niklas Dahl

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320430142

  10. Letter To The Editors

    1. Top of page
    2. Masthead
    3. Obituary
    4. Obituarys
    5. Conference Report
    6. Articles
    7. Invited Editorial Comment
    8. Articles
    9. Letter to the Editor
    10. Articles
    11. Letter To The Editors
    12. Articles
    13. Letter To The Editors
    14. Articles
    15. Brief Clinical Reports
    16. Articles
  11. Articles

    1. Top of page
    2. Masthead
    3. Obituary
    4. Obituarys
    5. Conference Report
    6. Articles
    7. Invited Editorial Comment
    8. Articles
    9. Letter to the Editor
    10. Articles
    11. Letter To The Editors
    12. Articles
    13. Letter To The Editors
    14. Articles
    15. Brief Clinical Reports
    16. Articles
    1. Direct DNA analysis of fragile X syndrome in Spanish pedigrees (pages 282–290)

      Isabel Tejada, Etienne Mornet, Valérie Biancalana, Isabelle Oberlé, Joelle Boué, Jean-Louis Mandel and André Boué

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320430144

    2. Fragile X mental retardation and the iduronate sulphatase locus: Testing laird's model of Fra(X) inheritance (pages 299–306)

      A. Clarke, D. Bradley, K. Gillespie, D. Rees, A. Holland and N. S. T. Thomas

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320430146

    3. Carrier detection of the fragile X syndrome with flanking RFLP markers and linkage analysis (pages 307–311)

      Marja-Leena Väisänen, Marketta Kähkönen and Jaakko Leisti

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320430147

    4. Linkage and risk assessment in fragile X families using new DNA Probes at Xq27 (pages 312–319)

      Dr. Nancy J. Carpenter, Jennifer Swartz-Boyd, Jane K. Prichard and Tan Lam

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320430148

    5. Validation of linkage-based DNA-diagnosis of fragile X gene carriers with the CGG repeat probe (pages 320–327)

      Dr. Bernard A. Van Oost, Arie P. T. Smits, Jos C. F. M. Dreesen, Ans M. W. van den Ouweland and Ben A. Oostra

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320430149

    6. New York State screening program for fragile X syndrome: A progress report (pages 328–332)

      Sarah L. Nolin, Donald A. Snider, Edmund C. Jenkins, Carl S. Dobkin, Kathleen Patchell, Michael Krawczun, Gloria Strong, Maryanne Colwell, Arnold Victor, Thomas Payyapilli, Marianne Turczyn, Anne Little, U. Nagaraja, Nancy Doyle, Barbara Kenefick and Connie Sullivan

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320430150

    7. Fragile X screening program in a spanish region (pages 333–338)

      Joaquina Gabarrón, Isabel Lopez, Guillermo Glover and Pablo Carbonell

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320430151

    8. Notes on the population genetics of fragile X syndrome (pages 339–344)

      Angela M. Vianna-Morgante and P. A. Otto

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320430152

    9. High prevalence of the Fra(X) syndrome cannot be explained by a high mutation rate (pages 345–352)

      Arie Smits, Dominique Smeets, Ben Hamel, Jos Dreesen and Bernard van Oost

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320430153

  12. Letter To The Editors

    1. Top of page
    2. Masthead
    3. Obituary
    4. Obituarys
    5. Conference Report
    6. Articles
    7. Invited Editorial Comment
    8. Articles
    9. Letter to the Editor
    10. Articles
    11. Letter To The Editors
    12. Articles
    13. Letter To The Editors
    14. Articles
    15. Brief Clinical Reports
    16. Articles
    1. Study of individuals possibly affected with the fragile X syndrome in a large swedish family in the 18th to 20th centuries (pages 353–354)

      Ulf Drugge, GöSta Holmgren, Hans Kison Blomquist, Niklas Dahl, Karl-Henrik Gustavson and Helena Malmgren

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320430154

  13. Articles

    1. Top of page
    2. Masthead
    3. Obituary
    4. Obituarys
    5. Conference Report
    6. Articles
    7. Invited Editorial Comment
    8. Articles
    9. Letter to the Editor
    10. Articles
    11. Letter To The Editors
    12. Articles
    13. Letter To The Editors
    14. Articles
    15. Brief Clinical Reports
    16. Articles
    1. Collaborative prospective study of the fragile X syndrome: One-year progress report (pages 355–360)

      S. L. Sherman, G. Barbi, K. Brøndum-Nielsen, W. T. Brown, N. J. Carpenter, A. E. Chudley, O. P. Ferraz, P. Ferreira, K-H. Gustavson, J. Halliday, A. Hockey, P. N. Howard-Peebles, E. Jenkins, I. Kennerknecht, M. Kähkönen, P. Ladaïque, J. Leisti, A. Maddalena, T. Mazurczak, J-F. Mattei, T. Mattina, M. J. McKinley, P. Murphy, M. C. Pellissier, S. Purvis-Smith, H. Robinson, U. Scapagnini, T. Schaap, L. R. Shapiro, A. P. T. Smits, P. Steinbach, G. Turner, I. A. Uchida, B. A. Van Oost, M-A. Voelckel, D. D. Weaver and T. Webb

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320430155

    2. Penetrance estimate of the Fra(X) gene using pointer versus direct estimate (pages 361–364)

      A. F. J. de Haan, A. P. T. Smits, D. F. C. M. Smeets and B. A. van Oost

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320430156

    3. Penetrance of Fra(X) gene: Influence of grandparental origin of the gene, mental status of the carrier mother, and presence of a normal transmitting male (pages 365–372)

      Arie P. T. Smits, Bernard A. van Oost, Anton F. J. de Haan, Ben C. J. Hamel, Jos C. F. M. Dreesen and Dominique F. C. M. Smeets

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320430157

    4. XLMR genes: Update 1992 (pages 373–382)

      Giovanni Neri, Pietro Chiurazzi, Fernando Arena, Herbert A. Lubs and Ian A. Glass

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320430158

    5. Nomenclature guidelines for X-linked mental retardation (pages 383–391)

      J. C. Mulley, B. Kerr, R. Stevenson and H. Lubs

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320430159

    6. Localization of non-specific X-linked mental retardation genes (pages 392–401)

      Dr. Bronwyn Kerr, Agi Gedeon, John Mulley and Gillian Turner

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320430160

    7. MASA syndrome: Delineation of the clinical spectrum at prepubertal age (pages 402–407)

      J. P. Fryns, C. Schrander-Stumpel, C. De Die-Smulders, M. Borghgraef and H. Van Den Berghe

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320430161

    8. Clasped-thumb mental retardation (MASA) syndrome: Confirmation of linkage to Xq28 (pages 408–414)

      Vincent R. Macias, Donald W. Day, Teresa E. King and Golder N. Wilson

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320430162

    9. Simpson-golabi-behmel syndrome associated with renal dysplasia and embryonal tumor: Localization of the gene to Xqcen-q21 (pages 428–435)

      Dr. Rhiannon M. Hughes-Benzie, Alasdair G. W. Hunter, Judith E. Allanson and Alex E. Mackenzie

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320430165

    10. Linkage of nonspecific X-linked mental retardation to Xq21.31 (pages 436–442)

      Kerry B. Jedele, Virginia V. Michels, Daniel J. Schaid, Karen V. Schowalter and Stephen N. Thibodeau

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320430166

    11. Congenital X-linked ataxia, progressive myoclonic encephalopathy, macular degeneration and recurrent infections (pages 443–451)

      Enrico Bertini, Raffaella Cusmai, Genevieve de Saint Basile, Françoise Le Deist, Matteo Di Capua, Di Roberto Gaggero, Carlo Dionisi-Vici, Clemente Santillo and Maurizio Caniglia

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320430167

  14. Brief Clinical Reports

    1. Top of page
    2. Masthead
    3. Obituary
    4. Obituarys
    5. Conference Report
    6. Articles
    7. Invited Editorial Comment
    8. Articles
    9. Letter to the Editor
    10. Articles
    11. Letter To The Editors
    12. Articles
    13. Letter To The Editors
    14. Articles
    15. Brief Clinical Reports
    16. Articles
    1. New XLMR syndrome with characteristic face, hypogenitalism, congenital hypotonia and pachygyria (pages 452–457)

      M. Zollino, P. Mastroiacovo, G. Zampino, P. Mariotti and G. Neri

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320430168

  15. Articles

    1. Top of page
    2. Masthead
    3. Obituary
    4. Obituarys
    5. Conference Report
    6. Articles
    7. Invited Editorial Comment
    8. Articles
    9. Letter to the Editor
    10. Articles
    11. Letter To The Editors
    12. Articles
    13. Letter To The Editors
    14. Articles
    15. Brief Clinical Reports
    16. Articles
    1. New X-linked syndrome with seizures, acquired micrencephaly, and agenesis of the corpus callosum (pages 458–466)

      Virginia K. Proud, Clive Levine and Nancy J. Carpenter

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320430169

    2. MRX8: An X-linked mental retardation condition with linkage to Xq21 (pages 467–474)

      Charles E. Schwartz, Melanie May, Tim Huang, David Ledbetter, Gail Anderson, David F. Barker, Hebert A. Lubs, Fernando Arena and Roger E. Stevenson

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320430170

    3. X-linked mental retardation and characteristic physical features in two brothers with duplication Xp22-Xpter (pages 475–478)

      Carlo Cianchetti, Francesco Muntoni, Angela-Maria Falchi, Annalisa Nucaro, Giuseppina Sannio-Fancello, Antonio Cao and Maria-Giovanna Marrosu

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320430171

    4. Spastic paraplegia with iron deposits in the basal ganglia: A new X-linked mental retardation syndrome (pages 479–490)

      J. Fernando Arena, Charles Schwartz, Roger Stevenson, Laura Lawrence, Anna Carpenter, Ranjan Duara, David Ledbetter, Tim Huang, Thomas Lehner, Jurg Ott and Herbert A. Lubs

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320430172

    5. Allan-herndon-dudley syndrome: Clinical and linkage studies on a second family (pages 491–497)

      Dr. Martin G. Bialer, Laura Lawrence, Roger E. Stevenson, Gittel Silverberg, Marjorie K. Williams, J. Fernando Arena, Herbert A. Lubs and Charles E. Schwartz

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320430173

    6. Neuropsychological studies in families with fragile-X negative X-linked mental retardation (pages 505–509)

      Carlo Cianchetti, Giuseppina Sannio-Fancello, Anna-Lisa Fratta, Maria-Paola Pischedda, Gabriella Spinicci, Maria-Giovanna Marrosu and Giorgio Filippi

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320430175

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