American Journal of Medical Genetics

Cover image for American Journal of Medical Genetics

1 May 1991

Volume 39, Issue 2

Pages fmi–fmi, 125–241

Currently known as: American Journal of Medical Genetics Part A

  1. Masthead

    1. Top of page
    2. Masthead
    3. Articles
    4. New Syndrome
    5. Articles
    6. Letter to the Editors
    7. Letter to Editors
    8. Letter to the Editors
    9. Letter to Editors
    10. Letter to the Editors
    1. You have free access to this content
      Masthead (page fmi)

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320390201

  2. Articles

    1. Top of page
    2. Masthead
    3. Articles
    4. New Syndrome
    5. Articles
    6. Letter to the Editors
    7. Letter to Editors
    8. Letter to the Editors
    9. Letter to Editors
    10. Letter to the Editors
    1. Hereditary hypotrichosis of the scalp (pages 125–129)

      Dr. Russell O. Hess and Hideo Uno

      Version of Record online: 6 JUN 2005 | DOI: 10.1002/ajmg.1320390202

    2. Mother and son with deletion of 3p25-pter (pages 130–132)

      J. Tazelaar, J. Roberson, D. L. Van Dyke, V. R. Babu and Dr. L. Weiss

      Version of Record online: 6 JUN 2005 | DOI: 10.1002/ajmg.1320390203

    3. X-linked syndrome: Mental retardation, hip luxation, and G6PD variant [Gd(+) Butantan] (pages 133–136)

      R. C. Stocco dos Santos, O. C. O. Barretto, K. Nonoyama, N. H. C. Castro, O. P. Ferraz, J. Walter-Moura, C. C. S. Vescio and W. Beçak

      Version of Record online: 6 JUN 2005 | DOI: 10.1002/ajmg.1320390204

    4. Cardio-Facio-cutaneous (CFC) syndrome: Report of two patients without hyperkeratotic skin lesions (pages 144–147)

      Dr. Yukihisa Matsuda, Ichiro Murano, Osamu Kondoh, Kiyosato Matsuo and Tadashi Kajii

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320390206

    5. Estimating genetic influences on the age-at-menarche: A survival analysis approach (pages 148–154)

      Joanne M. Meyer, Lindon J. Eaves, Andrew C. Heath and Nicholas G. Martin

      Version of Record online: 6 JUN 2005 | DOI: 10.1002/ajmg.1320390207

    6. Partial deletion of chromosome 6p: Delineation of the syndrome (pages 155–160)

      Catherine G. Palmer, Patricia Bader, Marilyn L. Slovak, David E. Comings and Mark J. Pettenati

      Version of Record online: 6 JUN 2005 | DOI: 10.1002/ajmg.1320390208

    7. Congenital nystagmus in a (46, XX/45,X) mosaic woman from a family with X-linked congenital nystagmus (pages 167–169)

      David H. Gutmann, Michael L. Brooks, Beverly S. Emanuel, Donna M. McDonald-McGinn and Dr. Elaine H. Zackai

      Version of Record online: 6 JUN 2005 | DOI: 10.1002/ajmg.1320390210

  3. New Syndrome

    1. Top of page
    2. Masthead
    3. Articles
    4. New Syndrome
    5. Articles
    6. Letter to the Editors
    7. Letter to Editors
    8. Letter to the Editors
    9. Letter to Editors
    10. Letter to the Editors
    1. Sensorineural hearing loss, enamel hypoplasia, and nail abnormalities in sibs (pages 192–195)

      Audrey Heimler, Joyce E. Fox, Joel E. Hershey and Paul Crespi

      Version of Record online: 6 JUN 2005 | DOI: 10.1002/ajmg.1320390214

  4. Articles

    1. Top of page
    2. Masthead
    3. Articles
    4. New Syndrome
    5. Articles
    6. Letter to the Editors
    7. Letter to Editors
    8. Letter to the Editors
    9. Letter to Editors
    10. Letter to the Editors
    1. Characterization of deletions at the retinoblastoma locus in patients with bilateral retinoblastoma (pages 196–200)

      Kai Kloss, Petra Währisch, Valerie Greger, Elmar Messmer, Henning Fritze, Wolfgang Höpping, Eberhard Passarge and Dr. Bernhard Horsthemke

      Version of Record online: 6 JUN 2005 | DOI: 10.1002/ajmg.1320390215

    2. Familial dermographism (pages 201–203)

      Kerry B. Jedele and Dr. Virginia V. Michels

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320390216

    3. Interstitial deletion del(2)(q24q31) with a phenotype similar to del(2)(q31q33) (pages 204–206)

      Christine Wamsler, Bertram Müller, Gabriele Freyberger and Dr. Michael Schmid

      Version of Record online: 6 JUN 2005 | DOI: 10.1002/ajmg.1320390217

    4. Dandy–Walker malformation in the Meckel syndrome (pages 207–210)

      Dr. Richard Herriot, Lavinia A. Hallam and Elizabeth S. Gray

      Version of Record online: 6 JUN 2005 | DOI: 10.1002/ajmg.1320390218

    5. Genetic analysis of Huntington disease in Italy (pages 211–214)

      F. Ajmar, P. Mandich, E. Bellone and G. Abbruzzese

      Version of Record online: 6 JUN 2005 | DOI: 10.1002/ajmg.1320390219

    6. DiGeorge anomaly associated with 10p deletion (pages 215–216)

      Giuseppe Monaco, Claudio Pignata, Elena Rossi, Ornella Mascellaro, Sergio Cocozza and Filippo Ciccimarra

      Version of Record online: 6 JUN 2005 | DOI: 10.1002/ajmg.1320390220

    7. Presymptomatic, prenatal, and exclusion testing for Huntington disease using seven closely linked DNA markers (pages 217–222)

      Dr. Mette I. Skraastad, Aart Verwest, Egbert Bakker, Maria Vegter-van der Vlis, Inge van Leeuwen-Cornelisse, Raymund A. C. Roos, Peter L. Pearson and Gert-Jan B. van Ommen

      Version of Record online: 6 JUN 2005 | DOI: 10.1002/ajmg.1320390221

  5. Letter to the Editors

    1. Top of page
    2. Masthead
    3. Articles
    4. New Syndrome
    5. Articles
    6. Letter to the Editors
    7. Letter to Editors
    8. Letter to the Editors
    9. Letter to Editors
    10. Letter to the Editors
    1. New lethal acrofacial dysostosis syndrome (pages 223–224)

      Jean-Pierre Fryns and Alice Kleckowska

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320390222

    2. Scope of Alagille syndrome (page 225)

      Andrew Czeizel

      Version of Record online: 6 JUN 2005 | DOI: 10.1002/ajmg.1320390223

  6. Letter to Editors

    1. Top of page
    2. Masthead
    3. Articles
    4. New Syndrome
    5. Articles
    6. Letter to the Editors
    7. Letter to Editors
    8. Letter to the Editors
    9. Letter to Editors
    10. Letter to the Editors
    1. Chromosome 11q23.3-qter deletion and Alexander disease (page 226)

      Dr. David H. Gutmann

      Version of Record online: 6 JUN 2005 | DOI: 10.1002/ajmg.1320390224

    2. Response to Dr. David Gutmann (page 227)

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

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320390225

    3. Estimated frequency of urea cycle enzymopathies in Japan (pages 228–229)

      Noriyuki Nagata, Ichiro Matsuda and Kazuhiko Oyanagi

      Version of Record online: 6 JUN 2005 | DOI: 10.1002/ajmg.1320390226

  7. Letter to the Editors

    1. Top of page
    2. Masthead
    3. Articles
    4. New Syndrome
    5. Articles
    6. Letter to the Editors
    7. Letter to Editors
    8. Letter to the Editors
    9. Letter to Editors
    10. Letter to the Editors
    1. Another paracentric inversion of chromosome 18 (page 238)

      Judith Bell, Robyn Dunlop and Jennifer Bryan

      Version of Record online: 6 JUN 2005 | DOI: 10.1002/ajmg.1320390230

  8. Letter to Editors

    1. Top of page
    2. Masthead
    3. Articles
    4. New Syndrome
    5. Articles
    6. Letter to the Editors
    7. Letter to Editors
    8. Letter to the Editors
    9. Letter to Editors
    10. Letter to the Editors
    1. Acro-renal polytopic defect (page 239)

      Dr. Hardally R. Hegde, Alexander K. C. Leung and Wm. Lane M. Robson

      Version of Record online: 6 JUN 2005 | DOI: 10.1002/ajmg.1320390231

    2. Response to Drs. Hegde, Leung, and Robson (page 240)

      Richard M. Pauli and Heidi Luebke

      Version of Record online: 6 JUN 2005 | DOI: 10.1002/ajmg.1320390232

  9. Letter to the Editors

    1. Top of page
    2. Masthead
    3. Articles
    4. New Syndrome
    5. Articles
    6. Letter to the Editors
    7. Letter to Editors
    8. Letter to the Editors
    9. Letter to Editors
    10. Letter to the Editors

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