American Journal of Medical Genetics

Cover image for American Journal of Medical Genetics

June 1987

Volume 27, Issue 2

Pages fmi–fmi, 245–493

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. Letter to the Editors
    6. Articles
    7. Brief Clinical Reports
    8. Articles
    9. Brief Clinical Reports
    10. Articles
    11. Brief Clinical Reports
    12. Articles
    13. Letter to the Editors
    14. Book Review
    1. You have free access to this content
      Masthead (page fmi)

      Version of Record online: 9 JUN 2005 | DOI: 10.1002/ajmg.1320270201

  2. Articles

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Reports
    5. Letter to the Editors
    6. Articles
    7. Brief Clinical Reports
    8. Articles
    9. Brief Clinical Reports
    10. Articles
    11. Brief Clinical Reports
    12. Articles
    13. Letter to the Editors
    14. Book Review
    1. Multiple congenital anomalies associated with apparently normal maternal intake of vitamin A: A phenocopy of the isotretinoin syndrome? (pages 245–248)

      Dr. M. S. Lungarotti, D. Marinelli, T. Mariani, A. Calabro, John M. Opitz and James F. Reynolds

      Version of Record online: 9 JUN 2005 | DOI: 10.1002/ajmg.1320270202

    2. Familial correlations from genes and shared environment for urine, plasma, and intraerythrocytic sodium (pages 249–255)

      Dr. Steven C. Hunt, Mary M. Dadone, Roger R. Williams, Lily L. Wu, Jean B. Smith, Hiroshi Kuida, K. Owen Ash, John M. Opitz and James F. Reynolds

      Version of Record online: 9 JUN 2005 | DOI: 10.1002/ajmg.1320270203

    3. Isochromosome 12p mosaicism (Pallister mosaic aneuploidy or Pallister-Killian syndrome): Report of 11 cases (pages 257–274)

      Dr. James F. Reynolds, Art Daniel, Thaddeus E. Kelly, Susanne M. Gollin, Mark J. Stephan, John Carey, William N. Adkins, Mary Jane Webb, Florence Char, Jorge F. Jimenez, John M. Opitz and Giovanni Neri

      Version of Record online: 9 JUN 2005 | DOI: 10.1002/ajmg.1320270204

  3. Brief Clinical Reports

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Reports
    5. Letter to the Editors
    6. Articles
    7. Brief Clinical Reports
    8. Articles
    9. Brief Clinical Reports
    10. Articles
    11. Brief Clinical Reports
    12. Articles
    13. Letter to the Editors
    14. Book Review
  4. Letter to the Editors

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Reports
    5. Letter to the Editors
    6. Articles
    7. Brief Clinical Reports
    8. Articles
    9. Brief Clinical Reports
    10. Articles
    11. Brief Clinical Reports
    12. Articles
    13. Letter to the Editors
    14. Book Review
    1. Mosaic isochromosome 12p (pages 291–294)

      Richard M. Pauli, Renee A. Zeier, Gurbax S. Sekhon and James F. Reynolds

      Version of Record online: 9 JUN 2005 | DOI: 10.1002/ajmg.1320270207

  5. Articles

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Reports
    5. Letter to the Editors
    6. Articles
    7. Brief Clinical Reports
    8. Articles
    9. Brief Clinical Reports
    10. Articles
    11. Brief Clinical Reports
    12. Articles
    13. Letter to the Editors
    14. Book Review
    1. Dyssegmental dysplasias: Clinical, radiographic, and morphologic evidence of heterogeneity (pages 295–312)

      Dr. Kirk A. Aleck, Art Grix, Carol Clericuzio, Paige Kaplan, Gerald E. Adomian, Ralph Lachman, David L. Rimoin and Judith G. Hall

      Version of Record online: 9 JUN 2005 | DOI: 10.1002/ajmg.1320270208

    2. Radial ray defect and Duane anomaly: Report of a family with autosomal dominant transmission (pages 313–319)

      Dr. Kay D. MacDermot, Robin M. Winter and James F. Reynolds

      Version of Record online: 9 JUN 2005 | DOI: 10.1002/ajmg.1320270209

  6. Brief Clinical Reports

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Reports
    5. Letter to the Editors
    6. Articles
    7. Brief Clinical Reports
    8. Articles
    9. Brief Clinical Reports
    10. Articles
    11. Brief Clinical Reports
    12. Articles
    13. Letter to the Editors
    14. Book Review
    1. Prenatal ultrasound diagnosis of diastrophic dysplasia at 16 weeks (pages 321–324)

      Dr. Thomaz Rafael Gollop, Alberto Eigier, John M. Opitz and James F. Reynolds

      Version of Record online: 9 JUN 2005 | DOI: 10.1002/ajmg.1320270210

  7. Articles

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Reports
    5. Letter to the Editors
    6. Articles
    7. Brief Clinical Reports
    8. Articles
    9. Brief Clinical Reports
    10. Articles
    11. Brief Clinical Reports
    12. Articles
    13. Letter to the Editors
    14. Book Review
    1. ReCAP: The registry of cytogenetic abnormalities and phenylketonuria (pages 325–336)

      Dr. J. M. Friedman, Janet P. Smith, Barbara N. Lerner, Jean S. Helgeson, Patricia N. Howard-Peebles, Charles E. Mize, Susan G. Mize, William L. Singleton, M. Eileen Smith, John M. Opitz and James F. Reynolds

      Version of Record online: 9 JUN 2005 | DOI: 10.1002/ajmg.1320270211

    2. Epidemiology of ambiguous genitalia in South America (pages 337–343)

      Dr. Eduardo E. Castilla, lêda M. Orioli, Regina Lugarinho, Graca Dutra, John M. Opitz and James F. Reynolds

      Version of Record online: 9 JUN 2005 | DOI: 10.1002/ajmg.1320270212

    3. Mandibulofacial dysostosis (Treacher Collins syndrome): A new proposal for its pathogenesis (pages 359–372)

      Dr. Kathleen K. Sulik, Malcolm C. Johnston, Steven J. Smiley, Harold S. Speight, Bennie E. Jarvis, John M. Opitz and James F. Reynolds

      Version of Record online: 9 JUN 2005 | DOI: 10.1002/ajmg.1320270214

  8. Brief Clinical Reports

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Reports
    5. Letter to the Editors
    6. Articles
    7. Brief Clinical Reports
    8. Articles
    9. Brief Clinical Reports
    10. Articles
    11. Brief Clinical Reports
    12. Articles
    13. Letter to the Editors
    14. Book Review
    1. Possible prenatal hydantoin effect in a child born to a nonepileptic mother (pages 373–378)

      Bernard N. Chodirker, Dr. Albert E. Chudley, Martin H. Reed, T. V. N. Persaud, John M. Opitz and James F. Reynolds

      Version of Record online: 9 JUN 2005 | DOI: 10.1002/ajmg.1320270215

  9. Articles

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Reports
    5. Letter to the Editors
    6. Articles
    7. Brief Clinical Reports
    8. Articles
    9. Brief Clinical Reports
    10. Articles
    11. Brief Clinical Reports
    12. Articles
    13. Letter to the Editors
    14. Book Review
    1. The effects of storage of blood and isolated DNA on the integrity of DNA (pages 379–390)

      Linda Madisen, David I. Hoar, Catherine D. Holroyd, Margaret Crisp, Dr. M. E. Hodes and James F. Reynolds

      Version of Record online: 9 JUN 2005 | DOI: 10.1002/ajmg.1320270216

    2. Cytogenetic study in children chronically habituated to inhalation of volatile substances (pages 391–397)

      Dr. Fabio Salamanca-Gómez, Germania Moreta, Virginia Palma, Teresa Garcia, Carmen Navarrete, Carlos Caraza, Raúl Varela, Mikio Hiroishi, Moisés López, Silvia Hernández, Leonora Buentello, John M. Opitz and James F. Reynolds

      Version of Record online: 9 JUN 2005 | DOI: 10.1002/ajmg.1320270217

    3. Phenotypic variation in male-transmitted fragile X: Genetic inferences (pages 401–417)

      Dr. Danuta Z. Loesch, David A. Hay, Grant R. Sutherland, J. Halliday, C. Judge, G. C. Webb, John M. Opitz and James F. Reynolds

      Version of Record online: 9 JUN 2005 | DOI: 10.1002/ajmg.1320270219

    4. Genetic aspects of early chiidhood scoliosis (pages 419–424)

      Dr. J. M. Connor, A. N. Conner, R. A. C. Connor, J. L. Tolmie, B. Yeung, D. Goudie and James F. Reynolds

      Version of Record online: 9 JUN 2005 | DOI: 10.1002/ajmg.1320270220

    5. Linkage and genetic counselling for the fragile X using DNA probes 52A, F9, DX13, and ST14 (pages 435–448)

      John C. Mulley, Agi K. Gedeon, Kerry A. Thorn, Lyndall J. Bates, Grant R. Sutherland, John M. Opitz and James F. Reynolds

      Version of Record online: 9 JUN 2005 | DOI: 10.1002/ajmg.1320270222

    6. Gonadal function in patients with Down syndrome (pages 449–458)

      Ying-Hui H. Hsiang, Dr. Gary D. Berkovitz, Gail L. Bland, Claude J. Migeon, Andrew C. Warren, John M. Opitz and James F. Reynolds

      Version of Record online: 9 JUN 2005 | DOI: 10.1002/ajmg.1320270223

    7. Partial androgen resistance due to a distinctive qualitative defect of the androgen receptor (pages 459–466)

      Dr. Leonard Pinsky, Morris Kaufman, Lynne L. Levitsky and James F. Reynolds

      Version of Record online: 9 JUN 2005 | DOI: 10.1002/ajmg.1320270224

  10. Brief Clinical Reports

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Reports
    5. Letter to the Editors
    6. Articles
    7. Brief Clinical Reports
    8. Articles
    9. Brief Clinical Reports
    10. Articles
    11. Brief Clinical Reports
    12. Articles
    13. Letter to the Editors
    14. Book Review
    1. Herrmann-Opitz syndrome: Report of an affected fetus (pages 467–470)

      Dr. K. Anyane-Yeboa, J. Kasznica, J. Malin, J. Maidman, John M. Opitz and James F. Reynolds

      Version of Record online: 9 JUN 2005 | DOI: 10.1002/ajmg.1320270225

  11. Articles

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Reports
    5. Letter to the Editors
    6. Articles
    7. Brief Clinical Reports
    8. Articles
    9. Brief Clinical Reports
    10. Articles
    11. Brief Clinical Reports
    12. Articles
    13. Letter to the Editors
    14. Book Review
    1. Common fragile sites: Their prevalence in subjects with constitutional and acquired chromosomal instability (pages 471–482)

      Dr. Bruna Tedeschi, Berardino Porfirio, Patrizia Vernole, Daniela Caporossi, Bruno Dallapiccola, Benedetto Nicoletti and Giovanni Neri

      Version of Record online: 9 JUN 2005 | DOI: 10.1002/ajmg.1320270226

  12. Letter to the Editors

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Reports
    5. Letter to the Editors
    6. Articles
    7. Brief Clinical Reports
    8. Articles
    9. Brief Clinical Reports
    10. Articles
    11. Brief Clinical Reports
    12. Articles
    13. Letter to the Editors
    14. Book Review
    1. Monosomy 17 mosaicism in amniotic fluid cells (pages 483–486)

      Dr. Daniel G. Stetka, Elizabeth McPherson, Jerald Kuhn, Pauline Anderson, Lawrence J. Emrich, Marion R. Piedmonte and James F. Reynolds

      Version of Record online: 9 JUN 2005 | DOI: 10.1002/ajmg.1320270227

    2. Hypospadias in a consanguineous family (pages 487–489)

      Michael Tsur, Nehama Linder, Susanne Cappis, John M. Opitz and James F. Reynolds

      Version of Record online: 9 JUN 2005 | DOI: 10.1002/ajmg.1320270228

    3. Congenital anomalies and aberrant tissue bands (page 491)

      Raberta A. Pagon and James F. Reynolds

      Version of Record online: 9 JUN 2005 | DOI: 10.1002/ajmg.1320270229

  13. Book Review

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Reports
    5. Letter to the Editors
    6. Articles
    7. Brief Clinical Reports
    8. Articles
    9. Brief Clinical Reports
    10. Articles
    11. Brief Clinical Reports
    12. Articles
    13. Letter to the Editors
    14. Book Review

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