American Journal of Medical Genetics

Cover image for American Journal of Medical Genetics

December 1987

Volume 28, Issue 4

Pages fmi–fmi, 779–1026

Currently known as: American Journal of Medical Genetics Part A

  1. Masthead

    1. Top of page
    2. Masthead
    3. Conference Report
    4. Articles
    5. Brief Clinical Report
    6. Articles
    7. Letter to the Editors
    8. Book Review
    1. Masthead (page fmi)

      Article first published online: 4 JUN 2005 | DOI: 10.1002/ajmg.1320280401

  2. Conference Report

    1. Top of page
    2. Masthead
    3. Conference Report
    4. Articles
    5. Brief Clinical Report
    6. Articles
    7. Letter to the Editors
    8. Book Review
    1. You have free access to this content
      Second Annual Prader-Willi Syndrome Scientific Conference (pages 779–790)

      Dr. David H. Ledbetter, Frank Greenberg, Vanja A. Holm, Suzanne B. Cassidy, John M. Opitz and James F. Reynolds

      Article first published online: 4 JUN 2005 | DOI: 10.1002/ajmg.1320280402

  3. Articles

    1. Top of page
    2. Masthead
    3. Conference Report
    4. Articles
    5. Brief Clinical Report
    6. Articles
    7. Letter to the Editors
    8. Book Review
    1. Duplication of proximal 15q as a cause of Prader-Willi syndrome (pages 791–802)

      Anjana L. Pettigrew, Susanne M. Gollin, Frank Greenberg, Vincent M. Riccardi, Dr. David H. Ledbetter, John M. Opitz and James F. Reynolds

      Article first published online: 2 JUN 2005 | DOI: 10.1002/ajmg.1320280403

    2. Unique mosaicism in Prader-Labhart-Willi syndrome—a contiguous gene or aneuploidy syndrome? (pages 803–811)

      Dr. BG Kousseff, T Diamond, Y Essig, K Miller, T Tedesco, John M. Opitz, James F. Reynolds and David H. Ledbetter

      Article first published online: 2 JUN 2005 | DOI: 10.1002/ajmg.1320280404

    3. Deletions of proximal 15q without Prader-Willi syndrome (pages 813–820)

      Frank Greenberg, David H. Ledbetter, John M. Opitz and James F. Reynolds

      Article first published online: 2 JUN 2005 | DOI: 10.1002/ajmg.1320280405

    4. Sister chromatid exchange analysis in the Prader-Labhart-Willi syndrome (pages 821–827)

      Merlin G. Butler, Bonnie B. Jenkins, John M. Opitz, James F. Reynolds and David H. Ledbetter

      Article first published online: 2 JUN 2005 | DOI: 10.1002/ajmg.1320280406

    5. Is angelman syndrome an alternate result of del(15)(qllql3)? (pages 829–838)

      R. Ellen Magenis, Michael G. Brown, Deborah A. Lacy, Sarojini Budden, Stephen LaFranchi, John M. Opitz, James F. Reynolds and David H. Ledbetter

      Article first published online: 4 JUN 2005 | DOI: 10.1002/ajmg.1320280407

    6. Plasma immunoreactive β-melanocyte stimulating hormone (lipotro-pin) levels in individuals with prader-labhart-willi syndrome (pages 839–844)

      Merlin G. Butler, Bonnie B. Jenkins, David N. Orth, James F. Reynolds and David H. Ledbetter

      Article first published online: 2 JUN 2005 | DOI: 10.1002/ajmg.1320280408

    7. Neonatal diagnosis of Prader-Willi syndrome and its implications (pages 845–856)

      Frank Greenberg, Fred F. B. Elder, John M. Opitz, James F. Reynolds and David H. Ledbetter

      Article first published online: 4 JUN 2005 | DOI: 10.1002/ajmg.1320280409

    8. Steroid metabolic disturbances in Prader-Willi syndrome (pages 857–864)

      Fred I. Chasalow, Sandra L. Blethen, Judith G. Tobash, Darlene Myles, Merlin G. Butler, John M. Opitz, James F. Reynolds and David H. Ledbetter

      Article first published online: 4 JUN 2005 | DOI: 10.1002/ajmg.1320280410

    9. Linear growth response to exogenous growth hormone in Prader-Willi syndrome (pages 865–871)

      Phillip D. K. Lee, Darrell M. Wilson, Lois Rountree, Raymond L. Hintz, Ron G. Rosenfeld, James F. Reynolds and David H. Ledbetter

      Article first published online: 4 JUN 2005 | DOI: 10.1002/ajmg.1320280411

    10. Premature coronary artery atherosolerosis in a patient with Prader-Willi syndrome (pages 873–880)

      Andrew S. Lamb, William M. Johnson, John M. Opitz, James F. Reynolds and David H. Ledbetter

      Article first published online: 2 JUN 2005 | DOI: 10.1002/ajmg.1320280412

    11. Clinical comparison of 59 Prader-Willi patients with and without the 15(Q12) deletion (pages 881–887)

      Sharon L. Wenger, Jeanne M. Hanchett, Mark W. Steele, Beate V. Maier and Wendy L. Golden

      Article first published online: 4 JUN 2005 | DOI: 10.1002/ajmg.1320280413

    12. Rumination and vomiting in Prader-Willi syndrome (pages 889–895)

      Randell C. Alexander, Louise R. Greenswag, Arthur J. Nowak, John M. Opitz, James F. Reynolds and David H. Ledbetter

      Article first published online: 4 JUN 2005 | DOI: 10.1002/ajmg.1320280414

    13. Emotional symptoms in Prader-Willi syndrome adolescents (pages 897–905)

      Barbara Y. Whitman, Pasquale Accardo, John M. Opitz, James F. Reynolds and David H. Ledbetter

      Article first published online: 2 JUN 2005 | DOI: 10.1002/ajmg.1320280415

    14. Social skills training of Prader-Willi staff (pages 907–913)

      William Mitchell, Kaye V. Cook, John M. Opitz, James F. Reynolds and David H. Ledbetter

      Article first published online: 4 JUN 2005 | DOI: 10.1002/ajmg.1320280416

    15. Duchenne muscular dystrophy: Comparison among different racial groups (pages 925–929)

      Dr. Eliete Rabbi Bortolini, Mayana Zatz, John M. Opitz and James F. Reynolds

      Article first published online: 4 JUN 2005 | DOI: 10.1002/ajmg.1320280418

  4. Brief Clinical Report

    1. Top of page
    2. Masthead
    3. Conference Report
    4. Articles
    5. Brief Clinical Report
    6. Articles
    7. Letter to the Editors
    8. Book Review
    1. Choanal atresia and athelia: Methimazole teratogenicity or a new syndrome? (pages 931–934)

      Frank Greenberg, John M. Opitz and James F. Reynolds

      Article first published online: 4 JUN 2005 | DOI: 10.1002/ajmg.1320280419

  5. Articles

    1. Top of page
    2. Masthead
    3. Conference Report
    4. Articles
    5. Brief Clinical Report
    6. Articles
    7. Letter to the Editors
    8. Book Review
    1. Pathological confirmation of cystic fibrosis in the fetus following prenatal diagnosis (pages 935–947)

      A. Ornoy, J. Arnon, D. Katznelson, M. Granat, B. Caspi, J. Chemke, John M. Opitz and James F. Reynolds

      Article first published online: 4 JUN 2005 | DOI: 10.1002/ajmg.1320280420

    2. Genetic counselling in unexpected familial recurrence of achondroplasia (pages 949–954)

      Dr. P. Dodinval, B. Le Marec, John M. Opitz and James F. Reynolds

      Article first published online: 2 JUN 2005 | DOI: 10.1002/ajmg.1320280421

    3. Parental perceptions of the burden of genetic disease (pages 955–963)

      Edem E. Ekwo, Jae-On Kim, Carol A. Gosselink, John M. Opitz and James F. Reynolds

      Article first published online: 4 JUN 2005 | DOI: 10.1002/ajmg.1320280422

    4. A syndrome of mental retardation, short stature, hemolytic anemia, delayed puberty, and abnormal facial appearance: Similarities to a report of aldolase a deficiency (pages 965–970)

      J. A. Hurst, Dr. M. Baraitser, R. M. Winter, John M. Opitz and James F. Reynolds

      Article first published online: 4 JUN 2005 | DOI: 10.1002/ajmg.1320280423

    5. Tibial aplasia-ectrodactyly as variant expression of the Gollop-Wolfgang complex: Report of a Brazilian family (pages 971–980)

      A. Richieri-Costa, Decio Brunoni, José Laredo Filho, Silvana Kasinski, John M. Opitz and James F. Reynolds

      Article first published online: 4 JUN 2005 | DOI: 10.1002/ajmg.1320280424

    6. X chromosome aneuploidy in lymphocyte cultures from women with recurrent spontaneous abortions (pages 981–987)

      Dr. D. E. Horsman, F. J. Dill, B. C. McGillivray, D. K. Kalousek, John M. Opitz and James F. Reynolds

      Article first published online: 4 JUN 2005 | DOI: 10.1002/ajmg.1320280425

    7. Use of the G8 probe in predicting risk of Huntington disease (pages 989–997)

      Dr. Nancy E. Maestri, Terri H. Beaty, Susan E. Folstein, Deborah A. Meyers, John M. Opitz and James F. Reynolds

      Article first published online: 4 JUN 2005 | DOI: 10.1002/ajmg.1320280426

    8. An integrated microcomputer system to maintain a genetic register for Huntington disease (pages 999–1006)

      Mansoor Sarfarazi, Oliver W. J. Quarrell, Geoffrey Wolak, Peter S. Harper, John M. Opitz and James F. Reynolds

      Article first published online: 4 JUN 2005 | DOI: 10.1002/ajmg.1320280427

    9. Dermatoglyphic development on the volar pads of rats with chromosome abnormalities (pages 1007–1013)

      M. Okajima, T. H. Yosida, T. Ikeuchi, John M. Opitz and James F. Reynolds

      Article first published online: 2 JUN 2005 | DOI: 10.1002/ajmg.1320280428

  6. Letter to the Editors

    1. Top of page
    2. Masthead
    3. Conference Report
    4. Articles
    5. Brief Clinical Report
    6. Articles
    7. Letter to the Editors
    8. Book Review
    1. A first description of dyssegmental dysplasia (pages 1015–1016)

      Robert J. Gorlin and John M. Opitz

      Article first published online: 4 JUN 2005 | DOI: 10.1002/ajmg.1320280429

    2. Facial effects of fetal alcohol exposure: Assessment by photographs and morphometric analysis (pages 1017–1018)

      Marta Vitéz, John M. Opitz and James F. Reynolds

      Article first published online: 4 JUN 2005 | DOI: 10.1002/ajmg.1320280430

    3. Survival in liveborn infants with anencephaly (pages 1019–1020)

      P. A. Baird, A. D. Sadovnick, John M. Opitz and James F. Reynolds

      Article first published online: 2 JUN 2005 | DOI: 10.1002/ajmg.1320280431

    4. Abnormal phenotype in a child with a “balanced” translocation 8/12 in mosaic state (pages 1021–1023)

      R. Saura, M. Longy, F. Serville, O. Chokairi, M. F. Froute and Giovanni Neri

      Article first published online: 4 JUN 2005 | DOI: 10.1002/ajmg.1320280432

  7. Book Review

    1. Top of page
    2. Masthead
    3. Conference Report
    4. Articles
    5. Brief Clinical Report
    6. Articles
    7. Letter to the Editors
    8. Book Review

SEARCH

SEARCH BY CITATION