American Journal of Medical Genetics

Cover image for American Journal of Medical Genetics

July 1988

Volume 30, Issue 3

Pages fmi–fmi, 703–864, ii–iii

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. Brief Clinical Reports
    9. Invited Editorial Comments
    10. Articles
    11. Letter to the Editors
    12. Articles
    13. Announcements
    1. Masthead (page fmi)

      Version of Record online: 8 JUN 2005 | DOI: 10.1002/ajmg.1320300301

  2. Articles

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Reports
    5. Articles
    6. Brief Clinical Reports
    7. Articles
    8. Brief Clinical Reports
    9. Invited Editorial Comments
    10. Articles
    11. Letter to the Editors
    12. Articles
    13. Announcements
    1. Partial aniridia, cerebellar ataxia, and mental deficiency (gillespie syndrome) in two brothers (pages 703–708)

      Ehrenfried O. Wittig, Carlos A. Moreira, Dr. Newton Freire-Maia, Angela M. Vianna-Morgante, John M. Opitz and James F. Reynolds

      Version of Record online: 8 JUN 2005 | DOI: 10.1002/ajmg.1320300302

    2. Autosomal recessive Robinow-like syndrome with anterior chamber cleavage anomalies (pages 709–718)

      Howard M. Saal, Robert M. Greenstein, Paul J. Weinbaum and Dr. Andrew E. Poole

      Version of Record online: 8 JUN 2005 | DOI: 10.1002/ajmg.1320300303

    3. A child with sclerocornea, short limbs, short stature, and distinct facial appearance (pages 719–724)

      Elizabeth M. Thompson, Dr. Robin M. Winter, John M. Opitz and James F. Reynolds

      Version of Record online: 8 JUN 2005 | DOI: 10.1002/ajmg.1320300304

    4. Association of double nor variant with Turner syndrome (pages 725–732)

      Carolyn Jones, I. Ahmed, Michael R. Cummings and Dr Ira M. Rosenthal

      Version of Record online: 8 JUN 2005 | DOI: 10.1002/ajmg.1320300305

    5. Digital and palmar dermatoglyphics in Dementia of the Alzheimer type (pages 733–740)

      Dr. Jay S. Luxenberg, Chris C. Plato, Kathleen M. Fox, Robert P. Friedland, Stanley I. Rapoport and James F. Reynolds

      Version of Record online: 8 JUN 2005 | DOI: 10.1002/ajmg.1320300306

  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. Brief Clinical Reports
    9. Invited Editorial Comments
    10. Articles
    11. Letter to the Editors
    12. Articles
    13. Announcements
    1. Nager acrofacial dysostosis: Evidence for apparent heterogeneity (pages 741–746)

      Dr. David J. Goldstein, L. David Mirkin, John M. Opitz and James F. Reynolds

      Version of Record online: 8 JUN 2005 | DOI: 10.1002/ajmg.1320300307

  4. Articles

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Reports
    5. Articles
    6. Brief Clinical Reports
    7. Articles
    8. Brief Clinical Reports
    9. Invited Editorial Comments
    10. Articles
    11. Letter to the Editors
    12. Articles
    13. Announcements
    1. Cerebral abnormalities in the Neu-Laxova syndrome (pages 747–756)

      Dr. Tereza I. Ostrovskaya, Gennady I. Lazjuk, John M. Opitz and James F. Reynolds

      Version of Record online: 8 JUN 2005 | DOI: 10.1002/ajmg.1320300308

  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. Brief Clinical Reports
    9. Invited Editorial Comments
    10. Articles
    11. Letter to the Editors
    12. Articles
    13. Announcements
    1. Caudal deficiency sequence in 7q terminal deletion (pages 757–761)

      Constance Schrander-Stumpel, Jaap Schrander, Jean-Pierre Fryns, Guus Hamers, John M. Opitz and James F. Reynolds

      Version of Record online: 8 JUN 2005 | DOI: 10.1002/ajmg.1320300309

    2. An unusual bandlike web in an infant with lethal multiple pterygium syndrome (pages 763–769)

      Ursula G. Froster-Iskenius, Cynthia Curry, Margaret Philp, Dr. Judith G. Hall, John M. Opitz and James F. Reynolds

      Version of Record online: 8 JUN 2005 | DOI: 10.1002/ajmg.1320300310

  6. Articles

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Reports
    5. Articles
    6. Brief Clinical Reports
    7. Articles
    8. Brief Clinical Reports
    9. Invited Editorial Comments
    10. Articles
    11. Letter to the Editors
    12. Articles
    13. Announcements
    1. Peroxisomal disorders: Clinical commentary and future prospects (pages 771–792)

      Dr. Golder N. Wilson, Ronald D. Holmes, Amiya K. Hajra, John M. Opitz and James F. Reynolds

      Version of Record online: 8 JUN 2005 | DOI: 10.1002/ajmg.1320300311

    2. The Hand-Foot-Genital (Hand-Foot-Uterus) syndrome: Family report and update (pages 793–803)

      Dr. Fahed Halal, John M. Opitz and James F. Reynolds

      Version of Record online: 8 JUN 2005 | DOI: 10.1002/ajmg.1320300312

  7. Brief Clinical Reports

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Reports
    5. Articles
    6. Brief Clinical Reports
    7. Articles
    8. Brief Clinical Reports
    9. Invited Editorial Comments
    10. Articles
    11. Letter to the Editors
    12. Articles
    13. Announcements
    1. Trisomy 18 associated with ectopia cordis and occipital meningocele (pages 805–810)

      Dr. David Bick, Richard I. Markowitz, Arthur Horwich, John M. Opitz and James F. Reynolds

      Version of Record online: 8 JUN 2005 | DOI: 10.1002/ajmg.1320300313

  8. Invited Editorial Comments

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Reports
    5. Articles
    6. Brief Clinical Reports
    7. Articles
    8. Brief Clinical Reports
    9. Invited Editorial Comments
    10. Articles
    11. Letter to the Editors
    12. Articles
    13. Announcements
    1. Ectopia cordis, midline defects and chromosome abnormalities: An epidemiologic perspective (pages 811–817)

      Dr. Muin J. Khoury, José F. Cordero, Sonja Rasmussen and John M. Opitz

      Version of Record online: 8 JUN 2005 | DOI: 10.1002/ajmg.1320300314

  9. Articles

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Reports
    5. Articles
    6. Brief Clinical Reports
    7. Articles
    8. Brief Clinical Reports
    9. Invited Editorial Comments
    10. Articles
    11. Letter to the Editors
    12. Articles
    13. Announcements
    1. A mouse malformation mutant supplement to the London Dysmorphology Database (pages 819–820)

      Dr. R. M. Winter, John M. Opitz and James F. Reynolds

      Version of Record online: 8 JUN 2005 | DOI: 10.1002/ajmg.1320300315

    2. Absence of detectable chromosomal and molecular abnormalities in monozygotic twins discordant for the Wiedemann-Beckwith syndrome (pages 821–833)

      Craig E. Litz, Kimberly A. Taylor, J. S. Qiu, Ora H. Pescovitz, Dr. Bérengère De Martinville, John M. Opitz and James F. Reynolds

      Version of Record online: 8 JUN 2005 | DOI: 10.1002/ajmg.1320300316

  10. 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. Brief Clinical Reports
    9. Invited Editorial Comments
    10. Articles
    11. Letter to the Editors
    12. Articles
    13. Announcements
    1. Syndromic cryptophthalmos (pages 835–837)

      Martin G. Bialer, William G. Wilson and John M. Opitz

      Version of Record online: 8 JUN 2005 | DOI: 10.1002/ajmg.1320300317

    2. Response to Bialer and Wilson (page 839)

      Ioan T. Thomas, Jaime L. Frias and John M. Opitz

      Version of Record online: 8 JUN 2005 | DOI: 10.1002/ajmg.1320300318

    3. Inheritance of Cranio-Fronto-Nasal syndrome (pages 841–842)

      M. L. Kwee, Dr. D. Lindhout and John M. Opitz

      Version of Record online: 8 JUN 2005 | DOI: 10.1002/ajmg.1320300319

    4. Male excess among anatomically normal fetuses in spontaneous abortions (pages 843–844)

      Louis H. Honoré and John M. Opitz

      Version of Record online: 8 JUN 2005 | DOI: 10.1002/ajmg.1320300320

    5. Diprosopus, anencephaly, and facial clefting (page 845)

      Dr. Robert J. Gorlin, John M. Opitz and James F. Reynolds

      Version of Record online: 8 JUN 2005 | DOI: 10.1002/ajmg.1320300321

    6. Opitz Oculo-Genital-Laryngeal syndrome (Opitz BBB/G compound syndrome) (pages 847–849)

      Heddie O. Sedano, Robert J. Gorlin and John M. Opitz

      Version of Record online: 8 JUN 2005 | DOI: 10.1002/ajmg.1320300322

    7. The Opitz syndrome (page 851)

      Giovanni Neri and Marco Cappa

      Version of Record online: 8 JUN 2005 | DOI: 10.1002/ajmg.1320300323

  11. Articles

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Reports
    5. Articles
    6. Brief Clinical Reports
    7. Articles
    8. Brief Clinical Reports
    9. Invited Editorial Comments
    10. Articles
    11. Letter to the Editors
    12. Articles
    13. Announcements
    1. Atypical Menkes steely hair disease (pages 853–858)

      Judith A. Westman, Delphis C. Richardson, Owen M. Rennert, Grant Morrow III, John M. Opitz and James F. Reynolds

      Version of Record online: 8 JUN 2005 | DOI: 10.1002/ajmg.1320300324

  12. Announcements

    1. Top of page
    2. Masthead
    3. Articles
    4. Brief Clinical Reports
    5. Articles
    6. Brief Clinical Reports
    7. Articles
    8. Brief Clinical Reports
    9. Invited Editorial Comments
    10. Articles
    11. Letter to the Editors
    12. Articles
    13. Announcements
    1. You have free access to this content
      Announcements (pages ii–iii)

      Version of Record online: 8 JUN 2005 | DOI: 10.1002/ajmg.1320300326

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