American Journal of Medical Genetics

Cover image for American Journal of Medical Genetics

January 1990

Volume 35, Issue 1

Pages fmi–fmi, 1–151

Currently known as: American Journal of Medical Genetics Part A

  1. Masthead

    1. Top of page
    2. Masthead
    3. Articles
    4. Invited Editorial Comment
    5. Articles
    6. Brief Clinical Report
    7. Articles
    8. Obituary
    9. Letter to the Editors
    10. Rapid Publications
    1. Masthead (page fmi)

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320350101

  2. Articles

    1. Top of page
    2. Masthead
    3. Articles
    4. Invited Editorial Comment
    5. Articles
    6. Brief Clinical Report
    7. Articles
    8. Obituary
    9. Letter to the Editors
    10. Rapid Publications
    1. Dermatoglyphic analysis of autistic Basque children (pages 1–9)

      Dr. M. I. Arrieta, B. Martinez, B. Criado, A. Simón, L. Salazar and C. M. Lostao

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320350102

    2. Familial 5q11.2[RIGHTWARDS ARROW]q13.3 segmental duplication cosegregating with multiple anomalies, including schizophrenia (pages 10–13)

      Dr. Barbara C. McGillivray, Anne S. Bassett, Sylvie Langlois, Tapio Pantzar and Stephen Wood

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320350103

    3. Chromosome mosaicism in hypomelanosis of Ito (pages 14–17)

      Catherine L. Ritter, Mark W. Steele, Sharon L. Wenger and Bernard A. Cohen

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320350104

  3. Invited Editorial Comment

    1. Top of page
    2. Masthead
    3. Articles
    4. Invited Editorial Comment
    5. Articles
    6. Brief Clinical Report
    7. Articles
    8. Obituary
    9. Letter to the Editors
    10. Rapid Publications
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  4. Articles

    1. Top of page
    2. Masthead
    3. Articles
    4. Invited Editorial Comment
    5. Articles
    6. Brief Clinical Report
    7. Articles
    8. Obituary
    9. Letter to the Editors
    10. Rapid Publications
    1. Fragile X frequency in a mentally retarded population in Brazil (pages 22–27)

      Regina C. Mingroni-Netto, Carla Rosenberg, Angela M. Vianna-Morgante and Rita de Cássia M. Pavanello

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320350106

    2. Neuropsychological dysfunction among affected heterozygous fragile X females (pages 28–35)

      James P. Grigsby, Melinda B. Kemper, Randi J. Hagerman and Carol S. Myers

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320350107

    3. The central nervous system in the Apert syndrome (pages 36–45)

      M. Michael Cohen Jr. and Sven Kreiborg

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320350108

    4. Aberrant bronchi and cardiovascular anomalies (pages 46–54)

      Dr. Jane A. Evans

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320350109

    5. New manifestations of Neu-Laxova syndrome (pages 55–59)

      Dr. Naveed, C. S. Manjunath and Vijaya Sreenivas

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320350110

    6. Partial deletion of the long arm of chromosome 11 [del(11)(q23.3[RIGHTWARDS ARROW]qter)] with abnormal white matter (pages 60–63)

      Terrance D. Wardinsky, Ed Weinberger, Roberta A. Pagon, Sterling K. Clarren and Horace C. Thuline

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320350111

    7. Autosomal recessive Robinow syndrome (pages 64–68)

      Dr. Ahmad S. Teebi

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320350112

    8. Somatic development in cleidocranial dysplasia (pages 69–74)

      Birgit Leth Jensen

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320350113

    9. Counseling and decision dilemmas associated with fetal blood sampling (pages 75–78)

      Janet E. Ulm, Dinesh M. Shah, Vaithilingam G. Dev and John A. Phillips III

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320350114

    10. Chromosome 6q deletions: A report of two additional cases and a review of the literature (pages 79–84)

      D. R. McLeod, S. B. Fowlow, A. Robertson, D. Samcoe, I. Burgess and J. J. Hoo

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320350115

    11. Neonatal progeroid syndrome: More than one disease? (pages 91–94)

      James I. Hagadorn, William G. Wilson, W. Allen Hogge, Joseph H. Callicott and Ernest F. Beale

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320350117

  5. Brief Clinical Report

    1. Top of page
    2. Masthead
    3. Articles
    4. Invited Editorial Comment
    5. Articles
    6. Brief Clinical Report
    7. Articles
    8. Obituary
    9. Letter to the Editors
    10. Rapid Publications
    1. Ectro-amelia syndrome associated with an interstitial deletion of 7q (pages 95–99)

      Martha A. Morey and Rodney R. Higgins

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320350118

  6. Articles

    1. Top of page
    2. Masthead
    3. Articles
    4. Invited Editorial Comment
    5. Articles
    6. Brief Clinical Report
    7. Articles
    8. Obituary
    9. Letter to the Editors
    10. Rapid Publications
    1. Five landmarks in inbreeding studies (pages 118–120)

      Dr. Newton Freire-Maia

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320350122

    2. Clinical/Epidemiological analysis of malformations (pages 121–125)

      M. L. Martinez-Frías, M.D. J. L. Frías and J. Salvador

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320350123

    3. Mouse major histocompatibility complex (H-2) and fetal lung development: Implications for human pulmonary maturation (pages 126–131)

      Ching-Chum Hu, Dr. Tina F. Jaskoll, Cedric Minkin and Michael Melnick

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320350124

    4. Prenatal diagnosis of X-linked hypohidrotic ectodermal dysplasia by linkage analysis (pages 132–135)

      Jonathan Zonana, Albert Schinzel, Meena Upadhyaya, Nicholas S. T. Thomas, Ingrun Anton-Lamprecht and Peter S. Harper

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320350125

  7. Obituary

    1. Top of page
    2. Masthead
    3. Articles
    4. Invited Editorial Comment
    5. Articles
    6. Brief Clinical Report
    7. Articles
    8. Obituary
    9. Letter to the Editors
    10. Rapid Publications
  8. Letter to the Editors

    1. Top of page
    2. Masthead
    3. Articles
    4. Invited Editorial Comment
    5. Articles
    6. Brief Clinical Report
    7. Articles
    8. Obituary
    9. Letter to the Editors
    10. Rapid Publications
    1. An unusual cardiomelic syndrome (page 139)

      Peter Bowen

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320350127

    2. Reply to Dr. Bowen (page 140)

      Robert F. Stratton and W. Robert Morrow

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320350128

    3. Dry skin and extranumerary areolae (page 141)

      N. Freire-Maia and E. A. Chautard-Freire-Maia

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320350129

  9. Rapid Publications

    1. Top of page
    2. Masthead
    3. Articles
    4. Invited Editorial Comment
    5. Articles
    6. Brief Clinical Report
    7. Articles
    8. Obituary
    9. Letter to the Editors
    10. Rapid Publications
    1. Rett phenotype with X/autosome translocation: Possible mapping to the short arm of chromosome X (pages 142–147)

      Hubert Journal, Judith Melki, Catherine Turleau, Arnold Munnich and Jean de Grouchy

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320350130

    2. A de novo X; 3 translocation in Rett syndrome (pages 148–151)

      H. Y. Zoghbi, D. H. Ledbetter, R. Schultz, A. K. Percy and D. G. Glaze

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320350131

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