American Journal of Medical Genetics

Cover image for American Journal of Medical Genetics

28 August 1995

Volume 58, Issue 2

Pages fmi–fmi, 101–207

Currently known as: American Journal of Medical Genetics Part A

  1. Masthead

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Reports
    5. Articles
    6. New Syndrome
    7. Articles
    8. Letters to the Editor
    9. Articles
    10. Books Received
    1. You have free access to this content
      Masthead (page fmi)

      Version of Record online: 16 MAY 2005 | DOI: 10.1002/ajmg.1320580201

  2. Articles

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Reports
    5. Articles
    6. New Syndrome
    7. Articles
    8. Letters to the Editor
    9. Articles
    10. Books Received
    1. Monozygotic twins discordant for the russell-silver syndrome (pages 101–105)

      Wendy Bailey, Bradley Popovich and Kenneth Lee Jones

      Version of Record online: 16 MAY 2005 | DOI: 10.1002/ajmg.1320580202

    2. Congenital healed cleft lip (pages 106–112)

      Dr. Eduardo E. Castilla and María Luísa Martínez-Frías

      Version of Record online: 16 MAY 2005 | DOI: 10.1002/ajmg.1320580203

    3. Apparently new “anophthalmia-plus” syndrome in sibs (pages 113–114)

      Prof. Dr. Jean-Pierre Fryns, Eric Legius, Philippe Moerman, Kamiel Vandenberghe and Herman Van den Berghe

      Version of Record online: 16 MAY 2005 | DOI: 10.1002/ajmg.1320580204

    4. Mutations in PAX3 that cause Waardenburg syndrome type I: Ten new mutations and review of the literature (pages 115–122)

      Clinton T. Baldwin, Christopher F. Hoth, Roberto A. Macina and Aubrey Milunsky

      Version of Record online: 16 MAY 2005 | DOI: 10.1002/ajmg.1320580205

    5. Alopecia/mental retardation syndrome (pages 123–124)

      Vickie L. Hannig and George E. Tiller

      Version of Record online: 16 MAY 2005 | DOI: 10.1002/ajmg.1320580206

    6. Linkage of preaxial polydactyly type 2 to 7q36 (pages 128–135)

      Anne V. Hing, Cynthia Helms, Rachel Slaugh, Andrea Burgess, Jen C. Wang, Thomas Herman, S. Bruce Dowton and Helen Donis-Keller

      Version of Record online: 16 MAY 2005 | DOI: 10.1002/ajmg.1320580208

    7. Microdontia with severe microcephaly and short stature in two brothers: Osteodysplastic primordial dwarfism with dental findings (pages 136–142)

      Dr. Henry J. Lin, Gregory Y. Sue, Carol D. Berkowitz, Jo Anne Brasel and Ralph S. Lachman

      Version of Record online: 16 MAY 2005 | DOI: 10.1002/ajmg.1320580209

    8. Uniparental disomy in congenital disorders: A prospective study (pages 143–146)

      Dr. Noralane M. Lindor, Pamela S. Karnes, Virginia V. Michels, Gordon W. Dewald, Jean Goerss, Syed Jalal, Robert B. Jenkins, Gerard Vockley and Stephen N. Thibodeau

      Version of Record online: 16 MAY 2005 | DOI: 10.1002/ajmg.1320580210

    9. Maternal uniparental disomy of chromosome 2 in a baby with trisomy 2 mosaicism in amniotic fluid culture (pages 147–151)

      Kathleen Harrison, Katerina Eisenger, Kwame Anyane-Yeboa and Dr. Stephen Brown

      Version of Record online: 16 MAY 2005 | DOI: 10.1002/ajmg.1320580211

  3. Brief Clinical Reports

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Reports
    5. Articles
    6. New Syndrome
    7. Articles
    8. Letters to the Editor
    9. Articles
    10. Books Received
    1. Intestinal lymphangiectasia in a patient with Zellweger cerebrohepatorenal syndrome (pages 152–154)

      Güliz Erdem, Olcay Oran, Esin Kotiloğlu, Gülsev Kale, Meral Topçu and Yavuz Renda

      Version of Record online: 16 MAY 2005 | DOI: 10.1002/ajmg.1320580212

  4. Articles

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Reports
    5. Articles
    6. New Syndrome
    7. Articles
    8. Letters to the Editor
    9. Articles
    10. Books Received
  5. New Syndrome

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Reports
    5. Articles
    6. New Syndrome
    7. Articles
    8. Letters to the Editor
    9. Articles
    10. Books Received
    1. Radio-ulnar synostosis, short stature, microcephaly, scoliosis, and mental retardation (pages 159–160)

      Masato Tsukahara, Kiyosato Matsuo and Susumu Furukawa

      Version of Record online: 16 MAY 2005 | DOI: 10.1002/ajmg.1320580214

  6. Articles

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Reports
    5. Articles
    6. New Syndrome
    7. Articles
    8. Letters to the Editor
    9. Articles
    10. Books Received
    1. Fibrillin abnormalities and prognosis in marfan syndrome and related disorders (pages 169–176)

      Takeshi Aoyama, Uta Francke, Cheryll Gasner and Heinz Furthmayr

      Version of Record online: 16 MAY 2005 | DOI: 10.1002/ajmg.1320580216

    2. Characterization of genetic deletions in becker muscular dystrophy using monoclonal antibodies against a deletion-prone region of dystrophin (pages 177–186)

      Le Thiet Thanh, Nguyen Thi Man, S. Hori, C. A. Sewry, V. Dubowitz and G. E. Morris

      Version of Record online: 16 MAY 2005 | DOI: 10.1002/ajmg.1320580217

    3. Omphalocele and gastroschisis in Europe: A survey of 3 million births 1980–1990 (pages 187–194)

      E. Calzolari, F. Bianchi, H. Dolk and M. Milan

      Version of Record online: 16 MAY 2005 | DOI: 10.1002/ajmg.1320580218

  7. Letters to the Editor

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Reports
    5. Articles
    6. New Syndrome
    7. Articles
    8. Letters to the Editor
    9. Articles
    10. Books Received
    1. Clinical variability in neonatal progeroid syndrome (pages 195–196)

      Jia-Woei Hou and Tso-Ren Wang

      Version of Record online: 16 MAY 2005 | DOI: 10.1002/ajmg.1320580219

    2. Bethlem myopathy is not allelic to limb-girdle muscular dystrophy type 1A (pages 197–198)

      Marcy C. Speer, Larry H. Yamaoka, Jeffrey Stajich, Karen Lewis, Margaret A. Pericak-Vance, Rebecca Stacy, Rup Tandan and Timothy J. Fries

      Version of Record online: 16 MAY 2005 | DOI: 10.1002/ajmg.1320580220

    3. Melorheostosis and somatic mosaicism (page 199)

      Jean-Pierre Fryns

      Version of Record online: 16 MAY 2005 | DOI: 10.1002/ajmg.1320580221

  8. Articles

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Reports
    5. Articles
    6. New Syndrome
    7. Articles
    8. Letters to the Editor
    9. Articles
    10. Books Received
    1. Genetic mapping of the cleidocranial dysplasia (CCD) locus on chromosome band 6p21 to include a microdeletion (pages 200–205)

      Bruce D. Gelb, Ed Cooper, Michael Shevell and Robert J. Desnick

      Version of Record online: 16 MAY 2005 | DOI: 10.1002/ajmg.1320580222

  9. Books Received

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Reports
    5. Articles
    6. New Syndrome
    7. Articles
    8. Letters to the Editor
    9. Articles
    10. Books Received
    1. Books received (pages 206–207)

      Version of Record online: 16 MAY 2005 | DOI: 10.1002/ajmg.1320580223

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