American Journal of Medical Genetics

Cover image for American Journal of Medical Genetics

July 1987

Volume 27, Issue 3

Pages fmi–fmi, 495–748, i–i

Currently known as: American Journal of Medical Genetics Part A

  1. Masthead

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

      Version of Record online: 9 JUN 2005 | DOI: 10.1002/ajmg.1320270301

  2. Obituary

    1. Top of page
    2. Masthead
    3. Obituary
    4. Articles
    5. Brief Clinical Reports
    6. Articles
    7. Brief Clinical Reports
    8. Letter to the Editors
    9. Articles
    10. Announcements
    1. In memoriam (pages 495–496)

      Martinus F. Niermeijer

      Version of Record online: 9 JUN 2005 | DOI: 10.1002/ajmg.1320270302

  3. Articles

    1. Top of page
    2. Masthead
    3. Obituary
    4. Articles
    5. Brief Clinical Reports
    6. Articles
    7. Brief Clinical Reports
    8. Letter to the Editors
    9. Articles
    10. Announcements
    1. Tetrasomy 9p caused by idic (9) (pter[RIGHTWARDS ARROW]q13[RIGHTWARDS ARROW]pter) (pages 497–503)

      Dr. Denise Pontes Cavalcanti, Iris Ferrari, José Carlos Cabral de Almeida, João Monteiro de Pina Neto, José A. de Oliveira and James F. Reynolds

      Version of Record online: 9 JUN 2005 | DOI: 10.1002/ajmg.1320270303

    2. Congenital anomalies: Mortality and morbidity, burden and classification (pages 505–523)

      Chin S. Chung, Ntinos C. Myrianthopoulos, John M. Opitz and James F. Reynolds

      Version of Record online: 9 JUN 2005 | DOI: 10.1002/ajmg.1320270304

    3. The relationship between fetal hemoglobin and disease severity in children with sickle cell anemia (pages 525–535)

      Daniel J. Odenheimer, Sharada A. Sarnaik, Charles F. Whitten, Donald L. Rucknagel, Charles F. Sing, John M. Opitz and James F. Reynolds

      Version of Record online: 9 JUN 2005 | DOI: 10.1002/ajmg.1320270305

  4. Brief Clinical Reports

    1. Top of page
    2. Masthead
    3. Obituary
    4. Articles
    5. Brief Clinical Reports
    6. Articles
    7. Brief Clinical Reports
    8. Letter to the Editors
    9. Articles
    10. Announcements
    1. Walker-Warburg syndrome with cleft lip and cleft palate in two sibs (pages 537–541)

      Barbara K. Burton, Robert G. Dillard, R. Grey Weaver, John M. Opitz and James F. Reynolds

      Version of Record online: 9 JUN 2005 | DOI: 10.1002/ajmg.1320270306

  5. Articles

    1. Top of page
    2. Masthead
    3. Obituary
    4. Articles
    5. Brief Clinical Reports
    6. Articles
    7. Brief Clinical Reports
    8. Letter to the Editors
    9. Articles
    10. Announcements
    1. Animal model: Dysmorphogenesis and death in a chicken embryo model (pages 543–552)

      Dr. Robert M. Fineman, Gary C. Schoenwolf and David J. Prieur

      Version of Record online: 9 JUN 2005 | DOI: 10.1002/ajmg.1320270307

    2. Phenotypic spectrum of 45,X/46,XY individuals (pages 553–559)

      Carla Rosenberg, O. Frota-Pessoa, Angela M. Vianna-Morgante, T. H. Chu, John M. Opitz and James F. Reynolds

      Version of Record online: 9 JUN 2005 | DOI: 10.1002/ajmg.1320270308

    3. Frequency of carriers of chronic (type I) Gaucher disease in Ashkenazi Jews (pages 561–565)

      Dr. Yehuda Maloth, Sara Chazan, Dr. Avital Cnaan, Ilana Gelernter, Chaya Klibansky and James F. Reynolds

      Version of Record online: 9 JUN 2005 | DOI: 10.1002/ajmg.1320270309

    4. Microcephaly: Genetic counselling and antenatal diagnosis after the birth of an affected child (pages 583–594)

      Dr. J. L. Tolmie, Margaret McNay, J. B. P. Stephenson, D. Doyle, J. M. Connor, John M. Opitz and James F. Reynolds

      Version of Record online: 9 JUN 2005 | DOI: 10.1002/ajmg.1320270311

    5. Linkage analysis in spinopontine atrophy: Correlation or HLA linkage with phenotypic findings in hereditary ataxia (pages 595–602)

      Dr. Allen E. Bale, Sherri J. Bale, Sandra L. Schlesinger, Henry F. McFarland, John M. Opitz and James F. Reynolds

      Version of Record online: 9 JUN 2005 | DOI: 10.1002/ajmg.1320270312

    6. De novo X;Y translocation associated with imperforate anus and retinal pigmentary abnormalities (pages 603–611)

      Dr. Kathreen Johnston, Steven Schonberg, Victoria Littman, Teresa Gregory, Samuel Gelbart, James O'Donnell, David R. Cox, John M. Opitz and James F. Reynolds

      Version of Record online: 9 JUN 2005 | DOI: 10.1002/ajmg.1320270313

    7. Segregation and linkage analyses of dopamine-β-hydroxylase activity in a six-generation pedigree (pages 613–621)

      Alexander Asamoah, Alexander F. Wilson, Dr. Robert C. Elston, Edward Dalferes Jr., Gerald S. Berenson, John M. Opitz and James F. Reynolds

      Version of Record online: 9 JUN 2005 | DOI: 10.1002/ajmg.1320270314

    8. Delineation of the male phenotype in craniofrontonasal syndrome (pages 623–631)

      Colleen A. Morris, Janice C. Palumbos, John C. Carey, John M. Opitz and James F. Reynolds

      Version of Record online: 9 JUN 2005 | DOI: 10.1002/ajmg.1320270315

    9. Intrafamilial variability in lysosomal storage diseases (pages 633–638)

      Dr. Joël Zlotogora, John M. Opitz and James F. Reynolds

      Version of Record online: 9 JUN 2005 | DOI: 10.1002/ajmg.1320270316

    10. Do some patients with seckel syndrome have hematological problems and/or chromosome breakage? (pages 645–649)

      Dr. Merlin G. Butler, Bryan D. Hall, Ronald N. Maclean, Carmen B. Lozzio, John M. Opitz and James F. Reynolds

      Version of Record online: 9 JUN 2005 | DOI: 10.1002/ajmg.1320270318

    11. Urofacial (Ochoa) syndrome (pages 661–667)

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

      Version of Record online: 9 JUN 2005 | DOI: 10.1002/ajmg.1320270320

    12. Genetic ascertainment with heterogeneous risk (pages 669–682)

      Dr. Edmond A. Murphy, Deborah A. Meyers, Charles A. Rohde, John M. Opitz and James F. Reynolds

      Version of Record online: 9 JUN 2005 | DOI: 10.1002/ajmg.1320270321

    13. Waardenburg syndrome, Hirschsprung megacolon, and Marcus Gunn ptosis (pages 683–686)

      F. Meire, L. Standaert, Prof. J. J. De Laey, L. H. Zeng and Giovanni Neri

      Version of Record online: 9 JUN 2005 | DOI: 10.1002/ajmg.1320270322

    14. Duplication 7p in a family with t(7;11): Association with anomalies of the anterior cranial base (pages 687–692)

      Dr. J. Michael Odell, Joseph R. Siebert, Cynthia Bradley, Darrell Salk and James F. Reynolds

      Version of Record online: 9 JUN 2005 | DOI: 10.1002/ajmg.1320270323

    15. Sexual behavior and Down syndrome: The biological mechanism (pages 693–700)

      Dr. Patricia A. Martin-DeLeon, Mary B. Williams and James F. Reynolds

      Version of Record online: 9 JUN 2005 | DOI: 10.1002/ajmg.1320270324

    16. Interstitial deletion of chromosome 2 (p23p25) (pages 701–706)

      Dr. Victor B. Penchaszadeh, Patricia K. Dowling, Jessica G. Davis, Rina Schmidt, Raul A. Wapnir, John M. Opitz and James F. Reynolds

      Version of Record online: 9 JUN 2005 | DOI: 10.1002/ajmg.1320270325

    17. Deletion of 2p: A cytogenetic and clinical update (pages 707–710)

      Julie Neidich, Elaine Zackai, Margaret Aronson, Dr. Beverly S. Emanuel, John M. Opitz and James F. Reynolds

      Version of Record online: 9 JUN 2005 | DOI: 10.1002/ajmg.1320270326

    18. Isolation of human Y chromosomal major repetitive sequences from a flow-sorted Y chromosomal library (pages 711–717)

      Yutaka Nishioka, Estelle Lamothe, John M. Opitz and James F. Reynolds

      Version of Record online: 9 JUN 2005 | DOI: 10.1002/ajmg.1320270327

  6. Brief Clinical Reports

    1. Top of page
    2. Masthead
    3. Obituary
    4. Articles
    5. Brief Clinical Reports
    6. Articles
    7. Brief Clinical Reports
    8. Letter to the Editors
    9. Articles
    10. Announcements
    1. Pterygium colli medianum and midline cervical cleft: Midline anomalies in the sense of a developmental field defect (pages 719–723)

      Sönke Godbersen, Volker Heckel, Dr. H.-R. Wiedemann and John M. Opitz

      Version of Record online: 9 JUN 2005 | DOI: 10.1002/ajmg.1320270328

  7. Letter to the Editors

    1. Top of page
    2. Masthead
    3. Obituary
    4. Articles
    5. Brief Clinical Reports
    6. Articles
    7. Brief Clinical Reports
    8. Letter to the Editors
    9. Articles
    10. Announcements
    1. Comment on COVESDEM syndrome (page 725)

      Dr. Meinhard Robinow

      Version of Record online: 9 JUN 2005 | DOI: 10.1002/ajmg.1320270329

    2. Noonan and Klinefelter syndromes in a child (pages 727–728)

      Alain Verloes, Ornella Guidi, Jacques Frederic, Claude Lambotte, John M. Opitz and James F. Reynolds

      Version of Record online: 9 JUN 2005 | DOI: 10.1002/ajmg.1320270330

    3. Craniolacunia as the result of compression and decompression of the fetal skull (pages 729–730)

      Dr. William G. Wilson, Bennett A. Alford, Patricia T. Schnatterly and James F. Reynolds

      Version of Record online: 9 JUN 2005 | DOI: 10.1002/ajmg.1320270331

    4. A new DNA probe proximal to and closely linked to fragile X (pages 731–732)

      Dr. N. J. Carpenter, H. Veenema, E. Bakker, M. H. Hofker, P. L. Pearson, John M. Opitz and James F. Reynolds

      Version of Record online: 9 JUN 2005 | DOI: 10.1002/ajmg.1320270332

    5. Preclinical testing in Huntington disease (pages 733–734)

      Dr. M. Bloch, M. R. Hayden and John M. Opitz

      Version of Record online: 9 JUN 2005 | DOI: 10.1002/ajmg.1320270333

    6. Abdominal distension in Kaufman-McKusick syndrome (pages 735–736)

      J. P. Fryns and Ph. Moerman

      Version of Record online: 9 JUN 2005 | DOI: 10.1002/ajmg.1320270334

    7. Announcement of the national epidermolysis Bullosa registry (page 737)

      D. Martin Carter and John M. Opitz

      Version of Record online: 9 JUN 2005 | DOI: 10.1002/ajmg.1320270335

  8. Articles

    1. Top of page
    2. Masthead
    3. Obituary
    4. Articles
    5. Brief Clinical Reports
    6. Articles
    7. Brief Clinical Reports
    8. Letter to the Editors
    9. Articles
    10. Announcements
    1. Chromosome 20 deletion in multiple endocrine neoplasia type 2: Expanded double-blind studies (pages 739–748)

      V. Ramesh Babu, Daniel L. Van Dyke, Wendy L. Flejter, Charles E. Jackson, John M. Opitz, James F. Reynolds, John M. Opitz and James F. Reynolds

      Version of Record online: 9 JUN 2005 | DOI: 10.1002/ajmg.1320270336

  9. Announcements

    1. Top of page
    2. Masthead
    3. Obituary
    4. Articles
    5. Brief Clinical Reports
    6. Articles
    7. Brief Clinical Reports
    8. Letter to the Editors
    9. Articles
    10. Announcements
    1. Announcement (page i)

      Walther Vogel

      Version of Record online: 9 JUN 2005 | DOI: 10.1002/ajmg.1320270337

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