American Journal of Medical Genetics

Cover image for American Journal of Medical Genetics

October 1989

Volume 34, Issue 2

Pages fmi–fmi, 149–303

Currently known as: American Journal of Medical Genetics Part A

  1. Masthead

    1. Top of page
    2. Masthead
    3. Obituary
    4. Articles
    5. Comment
    6. Articles
    7. Invited Editorial
    8. Brief Clinical Reports
    9. Letter to the Editors
    10. Brief Clinical Reports
    11. Letter to the Editors
    12. Articles
    13. Letter to the Editors
    14. Articles
    15. Letter to the Editors
    16. Lettter To The Editors
    1. Masthead (page fmi)

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320340201

  2. Obituary

    1. Top of page
    2. Masthead
    3. Obituary
    4. Articles
    5. Comment
    6. Articles
    7. Invited Editorial
    8. Brief Clinical Reports
    9. Letter to the Editors
    10. Brief Clinical Reports
    11. Letter to the Editors
    12. Articles
    13. Letter to the Editors
    14. Articles
    15. Letter to the Editors
    16. Lettter To The Editors
    1. Charles W. Cotterman (pages 149–154)

      John M. Opitz

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320340202

  3. Articles

    1. Top of page
    2. Masthead
    3. Obituary
    4. Articles
    5. Comment
    6. Articles
    7. Invited Editorial
    8. Brief Clinical Reports
    9. Letter to the Editors
    10. Brief Clinical Reports
    11. Letter to the Editors
    12. Articles
    13. Letter to the Editors
    14. Articles
    15. Letter to the Editors
    16. Lettter To The Editors
    1. Heterogeneity of X-linked recessive (Spino)cerebellar ataxia with or without spastic diplegia (pages 155–158)

      Dr. Selçuk Apak, Memnune Yüksel, Meral Özmen, Nurçin Saka, Feyza Darendeliler and Gerhard Neuhäuser

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320340203

    2. Ullrich-Turner syndrome in an XY female fetus with deletion of the sex-determining portion of the Y chromosome (pages 159–162)

      Natalie Blagowidow, David C. Page, Dale Huff and Michael T. Mennuti

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320340204

    3. Hypothesis: Familial Mediterranean fever—A genetic disorder of the lipocortin family? (pages 163–167)

      M. Shohat, J. R. Korenberg, A. D. Schwabe and J. I. Rotter

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320340205

    4. Familial Mediterranean fever in Armenians: Autosomal recessive inheritance with high gene frequency (pages 168–172)

      David B. Rogers, Mordechai Shohat, Gloria M. Petersen, Joan Bickal, Jane Congleton, Arthur D. Schwabe and Jerome I. Rotter

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320340206

  4. Comment

    1. Top of page
    2. Masthead
    3. Obituary
    4. Articles
    5. Comment
    6. Articles
    7. Invited Editorial
    8. Brief Clinical Reports
    9. Letter to the Editors
    10. Brief Clinical Reports
    11. Letter to the Editors
    12. Articles
    13. Letter to the Editors
    14. Articles
    15. Letter to the Editors
    16. Lettter To The Editors
    1. You have free access to this content
      Thoughts on a manuscript (page 173)

      Dr. Frederick Hecht

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320340207

  5. Articles

    1. Top of page
    2. Masthead
    3. Obituary
    4. Articles
    5. Comment
    6. Articles
    7. Invited Editorial
    8. Brief Clinical Reports
    9. Letter to the Editors
    10. Brief Clinical Reports
    11. Letter to the Editors
    12. Articles
    13. Letter to the Editors
    14. Articles
    15. Letter to the Editors
    16. Lettter To The Editors
    1. Familial abdominal wall defects (pages 174–176)

      Douglas W. Hershey, Hanns C. Haesslein, Clifford C. Marr and John C. Adkins

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320340208

    2. VACTERL with hydrocephalus: Further delineation of the syndrome(s) (pages 177–182)

      Dr. Jane A. Evans, Leonie C. Stranc, Paige Kaplan and Alasdair G. W. Hunter

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320340209

    3. Duplication of 16q and deletion of 15q (pages 183–186)

      Dr. William L. Nyhan, James Mascarello, Bruce Barshop, Diane Doroski and Kurt Hirschhorn

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320340210

    4. Autism is not associated with the Fragile X syndrome (pages 187–193)

      Stewart Einfeld, Helen Molony and Wayne Hall

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320340211

    5. CAMFAK syndrome: A demyelinating inherited disease similar to Cockayne syndrome (pages 194–198)

      Dr. Dinesh Talwar and Stephen A. Smith

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320340212

    6. Oliver McFarlane Syndrome: A 25-year follow-up (pages 199–201)

      Dr. J. R. Sampson, J. L. Tolmie and J. S. Cant

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320340213

    7. Intermittent thrombocytopenia and absent radii: Report of a patient with additional unusual manifestations (pages 202–206)

      Dr. Arie van Haeringen, Foekje Veenstra, Petra D. Maaswinkel-Mooij and Jacques J. P. van de Kamp

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320340214

    8. Antenatal diagnosis of 45,X/48,XYYY (pages 207–210)

      Christine R. Bryke, Maurice J. Mahoney and Teresa L. Yang-Feng

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320340215

    9. Genetic diagnosis of the preimplantation embryo (pages 211–216)

      John E. Buster and Dr. Sandra A. Carson

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320340216

    10. Hereditary retinal vasculopathy with cerebral white matter lesions (pages 217–220)

      Dr. David H. Gutmann, Kenneth H. Fischbeck and Robert C. Sergott

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320340217

    11. “Vascular Neurofibromatosis” and infantile Gangrene (pages 221–226)

      Dr. Boris G. Kousseff and Enid F. Gilbert-Barness

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320340218

    12. “New” ectodermal dysplasia syndrome with distinctive facial appearance and preaxial polydactyly of feet (pages 227–229)

      William G. Wilson, Kenneth E. Greer, Andrew B. Martof, Joan McIlhenny and Dennis L. Hatter

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320340219

    13. Translocation t(5;11)(q13.1;p13) associated with familial isolated aniridia (pages 230–232)

      Mark J. Pettenati, R. Grey Weaver and Barbara K. Burton

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320340220

    14. Dermatoglyphics in von Recklinghausen neurofibromatosis (pages 233–236)

      Rosanna Pallotta, Gaetana Carlone, Altea Petrucci and Francesco Chiarelli

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320340221

  6. Invited Editorial

    1. Top of page
    2. Masthead
    3. Obituary
    4. Articles
    5. Comment
    6. Articles
    7. Invited Editorial
    8. Brief Clinical Reports
    9. Letter to the Editors
    10. Brief Clinical Reports
    11. Letter to the Editors
    12. Articles
    13. Letter to the Editors
    14. Articles
    15. Letter to the Editors
    16. Lettter To The Editors
  7. Brief Clinical Reports

    1. Top of page
    2. Masthead
    3. Obituary
    4. Articles
    5. Comment
    6. Articles
    7. Invited Editorial
    8. Brief Clinical Reports
    9. Letter to the Editors
    10. Brief Clinical Reports
    11. Letter to the Editors
    12. Articles
    13. Letter to the Editors
    14. Articles
    15. Letter to the Editors
    16. Lettter To The Editors
    1. Otocephaly-midline malformation association (pages 246–249)

      Dr. Joseph H. Hersh, Richard H. McChane, Ellen M. Rosenberg, William H. Powers Jr., Cynthia Corrigan and Leslie Pancratz

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320340223

  8. Letter to the Editors

    1. Top of page
    2. Masthead
    3. Obituary
    4. Articles
    5. Comment
    6. Articles
    7. Invited Editorial
    8. Brief Clinical Reports
    9. Letter to the Editors
    10. Brief Clinical Reports
    11. Letter to the Editors
    12. Articles
    13. Letter to the Editors
    14. Articles
    15. Letter to the Editors
    16. Lettter To The Editors
    1. Response by Dr. Townes to Dr. Benke (page 251)

      Philip L. Townes

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320340225

  9. Brief Clinical Reports

    1. Top of page
    2. Masthead
    3. Obituary
    4. Articles
    5. Comment
    6. Articles
    7. Invited Editorial
    8. Brief Clinical Reports
    9. Letter to the Editors
    10. Brief Clinical Reports
    11. Letter to the Editors
    12. Articles
    13. Letter to the Editors
    14. Articles
    15. Letter to the Editors
    16. Lettter To The Editors
    1. Holoprosencephaly and interstitial deletion of 2(p2101p2109) (pages 252–254)

      Dr. William G. Wilson, Daniel E. Shanks, Kathryn W. Sudduth, Kathy A. Couper and Joan McIlhenny

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320340226

  10. Letter to the Editors

    1. Top of page
    2. Masthead
    3. Obituary
    4. Articles
    5. Comment
    6. Articles
    7. Invited Editorial
    8. Brief Clinical Reports
    9. Letter to the Editors
    10. Brief Clinical Reports
    11. Letter to the Editors
    12. Articles
    13. Letter to the Editors
    14. Articles
    15. Letter to the Editors
    16. Lettter To The Editors
  11. Articles

    1. Top of page
    2. Masthead
    3. Obituary
    4. Articles
    5. Comment
    6. Articles
    7. Invited Editorial
    8. Brief Clinical Reports
    9. Letter to the Editors
    10. Brief Clinical Reports
    11. Letter to the Editors
    12. Articles
    13. Letter to the Editors
    14. Articles
    15. Letter to the Editors
    16. Lettter To The Editors
    1. Holoprosencephaly: A developmental field defect (pages 258–264)

      Dr. Virginia P. Johnson

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320340228

  12. Letter to the Editors

    1. Top of page
    2. Masthead
    3. Obituary
    4. Articles
    5. Comment
    6. Articles
    7. Invited Editorial
    8. Brief Clinical Reports
    9. Letter to the Editors
    10. Brief Clinical Reports
    11. Letter to the Editors
    12. Articles
    13. Letter to the Editors
    14. Articles
    15. Letter to the Editors
    16. Lettter To The Editors
    1. Holoprosencephaly and cytogenetic findings: Further information (page 265)

      M. Michael Cohen Jr.

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320340229

    2. Agnathia, holoprosencephaly, and situs inversus (pages 266–267)

      Haynes B. Robinson Jr. and Roger Lenke

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320340230

  13. Articles

    1. Top of page
    2. Masthead
    3. Obituary
    4. Articles
    5. Comment
    6. Articles
    7. Invited Editorial
    8. Brief Clinical Reports
    9. Letter to the Editors
    10. Brief Clinical Reports
    11. Letter to the Editors
    12. Articles
    13. Letter to the Editors
    14. Articles
    15. Letter to the Editors
    16. Lettter To The Editors
    1. Prenatal detection of cyclopia associated with interstitial deletion of 2p (pages 268–270)

      Howard O. Grundy, Pam Niemeyer, Mahendra K. Rupani, Veronica F. Ward and Dr. E. Robert Wassman

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320340231

    2. Three sibs with achalasia and alacrimia: A separate entity different from triple-A syndrome (pages 289–291)

      F. Haverkamp, Dr. K. Zerres and R. Rosskamp

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320340233

  14. Letter to the Editors

    1. Top of page
    2. Masthead
    3. Obituary
    4. Articles
    5. Comment
    6. Articles
    7. Invited Editorial
    8. Brief Clinical Reports
    9. Letter to the Editors
    10. Brief Clinical Reports
    11. Letter to the Editors
    12. Articles
    13. Letter to the Editors
    14. Articles
    15. Letter to the Editors
    16. Lettter To The Editors
    1. Y chromosome mosaicism in 45, X turner syndrome (pages 294–296)

      Harry Ostrer and C. Mark Clayton

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320340235

    2. Situs inversus in conjoined twins (page 297)

      W. M. Layton

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320340236

    3. A different perspective on advanced parental age (page 298)

      Benjamin Rybicki

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320340237

    4. Reply to Dr. Rybicki (page 299)

      M. L. Martínez-Frías, J. Salvador and E. Rodríquez Pinilla

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320340238

    5. Availability of genetic services to the deaf (pages 300–301)

      Dr. Paul S. Ing, Melanie L. Lempke, Shelley D. Smith and William J. Kimberling

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320340239

  15. Lettter To The Editors

    1. Top of page
    2. Masthead
    3. Obituary
    4. Articles
    5. Comment
    6. Articles
    7. Invited Editorial
    8. Brief Clinical Reports
    9. Letter to the Editors
    10. Brief Clinical Reports
    11. Letter to the Editors
    12. Articles
    13. Letter to the Editors
    14. Articles
    15. Letter to the Editors
    16. Lettter To The Editors
    1. You have free access to this content
      Fragile X syndrome in females with autism (pages 302–303)

      Dr. Ira L. Cohen, W. Ted Brown, Edmund C. Jenkins, Michael S. Krawczun, Joseph H. French, Simchalam Raguthu, Enid G. Wolf-Schein, Vicki Sudhalter, Gene Fisch and Krystyna Wisniewski

      Version of Record online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320340240

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