American Journal of Medical Genetics

Cover image for American Journal of Medical Genetics

15 November 1994

Volume 53, Issue 3

Pages fmi–fmi, 207–305

Currently known as: American Journal of Medical Genetics Part A

  1. Masthead

    1. Top of page
    2. Masthead
    3. Brief Clinical Reports
    4. Articles
    5. Brief Clinical Reports
    6. Articles
    7. Letter to the Editors
    8. Books Received
    1. You have free access to this content
      Masthead (page fmi)

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320530301

  2. Brief Clinical Reports

    1. Top of page
    2. Masthead
    3. Brief Clinical Reports
    4. Articles
    5. Brief Clinical Reports
    6. Articles
    7. Letter to the Editors
    8. Books Received
    1. Polydactyly in a carrier of the gene for the meckel syndrome (pages 207–209)

      Dr. John Nelson, Norman C. Nevin and E. Jennifer Hanna

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320530302

  3. Articles

    1. Top of page
    2. Masthead
    3. Brief Clinical Reports
    4. Articles
    5. Brief Clinical Reports
    6. Articles
    7. Letter to the Editors
    8. Books Received
    1. Deformations in infants of diabetic and control pregnancies (pages 210–215)

      Dr. Margot I. Van Allen, Zane A. Brown, Barbara Plovie, Mary Lou Hanson and Robert H. Knopp

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320530303

  4. Brief Clinical Reports

    1. Top of page
    2. Masthead
    3. Brief Clinical Reports
    4. Articles
    5. Brief Clinical Reports
    6. Articles
    7. Letter to the Editors
    8. Books Received
  5. Articles

    1. Top of page
    2. Masthead
    3. Brief Clinical Reports
    4. Articles
    5. Brief Clinical Reports
    6. Articles
    7. Letter to the Editors
    8. Books Received
    1. Dermatoglyphic peculiarities in patients with Williams-Beuren syndrome (pages 227–235)

      Prof. Dr. Alexander Rodewald, Rainer Pankau, Angela Gosch and Armin Wessel

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320530306

    2. Sanfilippo syndrome type A in two adult sibs (pages 241–244)

      Noralane M. Lindor, Alan Hoffman, John F. O'Brien, Norman P. Hanson and Jerry N. Thompson

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320530308

    3. Non-immune hydrops fetalis associated with impaired fetal movement: A case report and review (pages 251–254)

      Nathaniel H. Robin, Mark T. Curtis, Wadia Mulla, Carol A. Reynolds, Endla Anday, Lucy B. Rorke and Elaine H. Zackai

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320530310

    4. Molecular analysis of a complex chromosomal rearrangement and a review of familial cases (pages 255–263)

      Denise A. S. Batista, G. Shashidhar Pai and Gail Stetten

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320530311

    5. Living history biography (pages 274–284)

      Theodore T. Puck

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320530313

    6. Confirmation that the conotruncal anomaly face syndrome is associated with a deletion within 22q11.2 (pages 285–289)

      Rumiko Matsuoka, Atsuyoshi Takao, Misa Kimura, Shin-ichiro Imamura, Chisato Kondo, Kunitaka Joh-o, Kazuo Ikeda, Makoto Nishibatake, Masahiko Ando and Kazuo Momma

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320530314

    7. Child with oral, facial, digital, and skeletal anomalies and psychomotor delay: A new ofds form? (pages 290–293)

      Orazio Gabrielli, Anna Ficcadenti, Giancarlo Fabrizzi, Paolo Perri, Antonio Mercuri, Giovanni V. Coppa and Pierluigi Giorgi

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320530315

    8. 18q− and 18q+ mosaicism in a mentally retarded boy (pages 296–299)

      Margreet G. E. M. Ausems, Shama L. Bhola, Cornelie A. Post-Blok, Raoul C. M. Hennekam and Henny F. de France

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320530317

  6. Letter to the Editors

    1. Top of page
    2. Masthead
    3. Brief Clinical Reports
    4. Articles
    5. Brief Clinical Reports
    6. Articles
    7. Letter to the Editors
    8. Books Received
    1. Lowry-MacLean syndrome does exist (pages 300–301)

      Boris G. Kousseff and Judith D. Ranells

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320530318

    2. Renal agenesis, multicystic dysplasia, and uretero-pelvic junction obstruction— a common pathogenesis? (page 302)

      Wm. Lane M. Robson, R. Curtis Rogers and Alexander K. C. Leung

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320530319

    3. Cayler cardiofacial syndrome and del22qll: Part of the CATCH22 phenotype (pages 303–304)

      Aldo Giannotti, Maria Cristina Digilio, Bruno Marino, Rita Mingarelli and Bruno Dallapiccola

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320530320

  7. Books Received

    1. Top of page
    2. Masthead
    3. Brief Clinical Reports
    4. Articles
    5. Brief Clinical Reports
    6. Articles
    7. Letter to the Editors
    8. Books Received
    1. Books Received (page 305)

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320530321

SEARCH

SEARCH BY CITATION