American Journal of Medical Genetics

Cover image for American Journal of Medical Genetics

February 1990

Volume 35, Issue 2

Pages fmi–fmi, 153–298

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. Brief Clinical Reports
    7. Articles
    8. 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.1320350201

  2. Articles

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Reports
    5. Articles
    6. Brief Clinical Reports
    7. Articles
    8. Letter to the Editors
    1. Geleophysic dysplasia (pages 153–156)

      James E. Wraith, Agnes Bankier, C. W. Chow, Dr. David M. Danks and Imdad B. Sardharwalla

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320350202

    2. Current assessment of fetal losses as a direct consequence of chorionic villus sampling (pages 174–177)

      James D. Goldberg, Alison E. Porter and Mitchell S. Golbus

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320350206

    3. Fetal loss rate after chorionic villus sampling and subsequent amniocentesis (pages 178–180)

      H. Brandenburg, M. G. J. Jahoda, L. Pijpers, A. Reuss, W. J. Kleyer and J. W. Wladimiroff

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320350207

    4. Direct chromosome preparation and culture using chorionic villi: An evaluation of the two techniques (pages 181–183)

      Giuseppe Simoni, Gianluigi Terzoli and Franca Rossella

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320350208

    5. Prospective study of amniocentesis performed between weeks 9 and 16 of gestation: Its feasibility, risks, complications and use in early genetic prenatal diagnosis (pages 188–196)

      B. Rafael Elejalde, Maria M. de Elejalde, Juan M. Acuña, Diana Thelen, Carlos Trujillo and Michael Karrmann

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320350210

    6. Preimplantation sexing and diagnosis of hypoxanthine phosphoribosyl transferase deficiency in mice by biochemical microassay (pages 201–205)

      Marilyn Monk, Alan Handyside, Audrey Muggleton-Harris and David Whittingham

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320350212

    7. Legal and ethical implications of fetal diagnosis and gene therapy (pages 215–218)

      George J. Annas and Sherman Elias

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320350214

  3. Brief Clinical Reports

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Reports
    5. Articles
    6. Brief Clinical Reports
    7. Articles
    8. Letter to the Editors
    1. Spondylocostal dysostosis: Dominant type (pages 219–221)

      Peter Lorenz and Edgar Rupprecht

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320350215

  4. Articles

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Reports
    5. Articles
    6. Brief Clinical Reports
    7. Articles
    8. Letter to the Editors
    1. Transcobalamin II deficiency presenting with methylmalonic aciduria and homocystinuria and abnormal absorption of cobalamin (pages 222–228)

      Bruce A. Barshop, Jon Wolff, Dr. William L. Nyhan, Alice Yu, Christina Prodanos, Gilbert Jones, Lawrence Sweetman, Jack Leslie, Jan Holm, Ralph Green, Donald W. Jacobsen, Bernard A. Cooper and David Rosenblatt

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320350216

    2. Mirror polydactyly: Pathogenesis based on a morphogen gradient theory (pages 229–235)

      Dr. Denis L. Viljoen and Susan H. Kidson

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320350217

    3. A ring X chromosome, 46,Y,r(X)(p22.33q28), as a cause of extreme short stature in a male (pages 241–244)

      Tsutomu Ogata, Nobutake Matsuo and Nobuyoshi Shimizu

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320350219

    4. Three-generation dominant transmission of the Silver-Russell syndrome (pages 245–250)

      Peter A. Duncan, Judith G. Hall, Lawrence R. Shapiro and Betsy K. Vibert

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320350220

    5. Congenital hypoplastic (Diamond-Blackfan) anemia in seven members of one kindred (pages 251–256)

      David H. Viskochil, John C. Carey, Bertil E. Glader, Gerald Rothstein and Robert D. Christensen

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320350221

    6. Comparison of education and occupation of adults with achondroplasia with same-sex sibs (pages 257–260)

      Dr. Nancy Roizen, Edem Ekwo and Carol Gosselink

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320350222

    7. Distal deletion of the short arm of chromosome 6 (pages 261–265)

      Vickie L. Zurcher, Wendy L. Golden and Arthur B. Zinn

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320350223

    8. Aspartoacylase deficiency and Canavan disease in Saudi Arabia (pages 266–268)

      Pinar T. Ozand, Generoso G. Gascon and Mohammed Dhalla

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320350224

    9. Loss of the 3p25.3 band is critical in the manifestation of del(3p) syndrome: Karyotype-phenotype correlation in cases with deficiency of the distal portion of the short arm of chromosome 3 (pages 269–273)

      Kouji Narahara, Kiyoshi Kikkawa, Masae Murakami, Kei Hiramoto, Hiroshi Namba, Kazushiro Tsuji, Yuji Yokoyama and Hiroshi Kimoto

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320350225

    10. Nonimmunologic hydrops fetalis: An etiopathogenetic approach through the postmortem study of 59 patients (pages 274–279)

      A. Ruiz Villaespesa, M. P. Suarez Mier, P. Lopez Ferrer, I. Alvarez Baleriola and Dr. J. I. Rodriguez Gonzalez

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320350226

    11. Mild form of Jeune syndrome in two sisters (pages 280–282)

      Prof. P. L. Giorgi, O. Gabrielli, V. Bonifazi, C. Catassi and G. V. Coppa

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320350227

  5. Brief Clinical Reports

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Reports
    5. Articles
    6. Brief Clinical Reports
    7. Articles
    8. Letter to the Editors
    1. Proteus syndrome: Course of a severe case (pages 283–285)

      Ariadne Malamitsi-Puchner, Dimitris Dimitriadis, Christos Bartsocas and H.-R. Wiedemann

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320350228

  6. Articles

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Reports
    5. Articles
    6. Brief Clinical Reports
    7. Articles
    8. Letter to the Editors
    1. Chromosome 7 abnormalities in parents of children with holoprosencephaly and hydronephrosis (pages 286–288)

      Dr. I. W. Lurie, H. G. Ilyina, L. V. Podleschuk, L. B. Gorelik and D. V. Zaletajev

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320350229

  7. Letter to the Editors

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Reports
    5. Articles
    6. Brief Clinical Reports
    7. Articles
    8. Letter to the Editors
    1. Craniosynostosis in the Ullrich-Turner syndrome (pages 289–290)

      M. Michael Cohen Jr.

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320350230

    2. Comments on Dr. Cohen's letter (page 292)

      John H. Diliberti

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320350232

    3. Excess of females in chromosomally normal spontaneous abortuses (pages 297–298)

      Dr. Iris Bartels, Ingo Hansmann and Bernd Eiben

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320350235

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