American Journal of Medical Genetics

Cover image for American Journal of Medical Genetics

June 1989

Volume 33, Issue 2

Pages fmi–fmi, 155–286

Currently known as: American Journal of Medical Genetics Part A

  1. Masthead

    1. Top of page
    2. Masthead
    3. Articles
    4. New Syndromes
    5. Articles
    6. Brief Clinical Reports
    7. Articles
    8. Brief Clinical Reports
    9. Articles
    10. New Syndromes
    11. Letter to the Editor
    1. Masthead (page fmi)

      Article first published online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320330201

  2. Articles

    1. Top of page
    2. Masthead
    3. Articles
    4. New Syndromes
    5. Articles
    6. Brief Clinical Reports
    7. Articles
    8. Brief Clinical Reports
    9. Articles
    10. New Syndromes
    11. Letter to the Editor
    1. Two rare developmental defects of the lower limbs with confirmation of the lewin and opitz hypothesis on the fibular and tibial developmental fields (pages 161–164)

      Lorenzo Pavone, Denis Viljoen, Salvatore Ardito, Renata Rizzo, Giovanni Neri, Gianfranco Longo and Peter Beighton

      Article first published online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320330203

    2. Femoral duplication: A case report (pages 165–169)

      Dr. Joann Bodurtha, Maria Coutinho, Richard Benator, Jay Nogi, Milton Sholley and Walter E. Nance

      Article first published online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320330204

    3. Humero-radio-ulnar synostosis: A new case and review (pages 170–171)

      Joseph H. Hersh, Margie R. Joyce and Laura E. Profumo

      Article first published online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320330205

    4. Aplasia of the tibia with bifurcation of the femur and ectrodactyly: Evidence for an autosomal recessive type (pages 172–175)

      Gertrude Kohn, Raghda El Shawwa and Michael Grunebaum

      Article first published online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320330206

    5. Humero-radial synostosis with ulnar defects in sibs (pages 176–179)

      Jeanette C. Ramer and Roger L. Ladda

      Article first published online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320330207

    6. Familial uterine hernia syndrome: Report of an Arab family with four affected males (pages 180–181)

      Dr. Kamal K. Naguib, Ahmad S. Teebi, Talaat I. Farag, Sadika A. Al-Awadi, Mohammed Y. El-Khalifa and El-Sayed Mahfouz

      Article first published online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320330208

    7. Slowly progressive macrocephaly with hamartomas: A new syndrome? (pages 182–185)

      Dr. Fahed Halal and Kenneth Silver

      Article first published online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320330209

  3. New Syndromes

    1. Top of page
    2. Masthead
    3. Articles
    4. New Syndromes
    5. Articles
    6. Brief Clinical Reports
    7. Articles
    8. Brief Clinical Reports
    9. Articles
    10. New Syndromes
    11. Letter to the Editor
    1. Ptosis of eyelids, strabismus, diastasis recti, hip defect, cryptorchidism, and developmental delay in two sibs (pages 186–189)

      Prof. Franco Carnevale, Grazyna Krajewska, Rita Fischetto, Maria Grazia Greco and Angelica Bonvino

      Article first published online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320330210

  4. Articles

    1. Top of page
    2. Masthead
    3. Articles
    4. New Syndromes
    5. Articles
    6. Brief Clinical Reports
    7. Articles
    8. Brief Clinical Reports
    9. Articles
    10. New Syndromes
    11. Letter to the Editor
    1. A case of the Freire-Maia odontotrichomelic syndrome: Nosology with EEC syndrome (pages 190–193)

      Prof. Lorenzo Pavone, Renata Rizzo, Alessandra Tiné, Giuseppe Micali, Giovanni Sorge and Giovanni Neri

      Article first published online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320330211

    2. Johanson-Blizzard syndrome: Clinical and pathological findings in 2 sibs (pages 194–199)

      Nevenka S. Gould, John B. Paton and Angela R. Bennett

      Article first published online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320330212

    3. Multivariate analysis of body shape in fragile X (Martin-Bell) syndrome (pages 200–208)

      Dr. Danuta Z. Loesch and Susan R. Wilson

      Article first published online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320330213

    4. Brachyolmia: Radiographic and genetic evidence of heterogeneity (pages 209–219)

      M. Shohat, R. Lachman, H. E. Gruber and D. L. Rimoin

      Article first published online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320330214

    5. Duplication of 5ql1.2[RIGHTWARDS ARROW]q13.1 from a familial (5;20) balanced insertion (pages 220–223)

      Moh-Ying Yip, John Kemp, Nils Hanson, Meredith Wilson, Stuart Purvis-Smith and P. R. L. Lam-Po-Tang

      Article first published online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320330215

    6. Osteodysplastic primordial dwarfism: Report of a further case with manifestations similar to those of types I and III (pages 224–227)

      Dr. E. A. Haan, M. E. Furness, S. Knowles, L. L. Morris, G. Scott, J. M. Svigos and R. Vigneswaren

      Article first published online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320330216

  5. Brief Clinical Reports

    1. Top of page
    2. Masthead
    3. Articles
    4. New Syndromes
    5. Articles
    6. Brief Clinical Reports
    7. Articles
    8. Brief Clinical Reports
    9. Articles
    10. New Syndromes
    11. Letter to the Editor
    1. Terminal deletion 4q in a severely retarded boy (pages 228–230)

      Dr. Maria I. de Michelena and Patricia J. Campos

      Article first published online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320330217

  6. Articles

    1. Top of page
    2. Masthead
    3. Articles
    4. New Syndromes
    5. Articles
    6. Brief Clinical Reports
    7. Articles
    8. Brief Clinical Reports
    9. Articles
    10. New Syndromes
    11. Letter to the Editor
    1. Familial distal arthrogryposis with craniofacial abnormalities: A new subtype of type II? (pages 231–237)

      Cynthia A. Moore and David D. Weaver

      Article first published online: 4 JUN 2005 | DOI: 10.1002/ajmg.1320330218

    2. Prenatal diagnosis of cystic fibrosis by using linked DNA markers in 138 pregnancies at l-in-4 risk (pages 238–241)

      G. L. Feldman, N. Lewiston, S. D. Fernbach, W. E. O'Brien, R. Williamson, B. J. Wainwright and A. L. Beaudet

      Article first published online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320330219

  7. Brief Clinical Reports

    1. Top of page
    2. Masthead
    3. Articles
    4. New Syndromes
    5. Articles
    6. Brief Clinical Reports
    7. Articles
    8. Brief Clinical Reports
    9. Articles
    10. New Syndromes
    11. Letter to the Editor
    1. Bilateral renal agenesis and Mullerian anomalies in a 47,XXX fetus (pages 242–243)

      W. Allen Hogge, Dan J. Vick, Patricia A. Schnatterly and R. Hunt MacMillan

      Article first published online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320330220

  8. Articles

    1. Top of page
    2. Masthead
    3. Articles
    4. New Syndromes
    5. Articles
    6. Brief Clinical Reports
    7. Articles
    8. Brief Clinical Reports
    9. Articles
    10. New Syndromes
    11. Letter to the Editor
    1. Epilepsy and clefting disorders: Lack of evidence of a familial association (pages 244–247)

      Jacqueline T. Hecht, J. Fred Annegers and Leonard T. Kurland

      Article first published online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320330221

    2. Estimation of fertility and fitness in Huntington disease in New England (pages 248–254)

      Carol A. Mastromauro, Gregory J. Meissen, L. Adrienne Cupples, Dan K. Kiely, Barbara Berkman and Richard H. Myers

      Article first published online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320330222

    3. Clinical, pathological, and biochemical studies on an infantile case of sulfatide/GM1 activator protein deficiency (pages 255–265)

      David A. Wenger, Gregory DeGala, Carolyn Williams, Harold A. Taylor, Roger E. Stevenson, James R. Pruitt, John Miller, Paul D. Garen and J. Douglas Balentine

      Article first published online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320330223

    4. “Acadian” and “classical” forms of Friedreich ataxia are most probably caused by mutations at the same locus (pages 266–268)

      Dr. Bronya J. B. Keats, Laura J. Ward, Jacqui Shaw, Aranda Wickremasinghe and Susan Chamberlain

      Article first published online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320330224

    5. Genetic aspects of artificial insemination with donor semen: The French CECOS federation guidelines (pages 269–275)

      Pierre Jalbert, Claude Leonard, Jacqueline Selva and Pr. Georges David

      Article first published online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320330225

  9. New Syndromes

    1. Top of page
    2. Masthead
    3. Articles
    4. New Syndromes
    5. Articles
    6. Brief Clinical Reports
    7. Articles
    8. Brief Clinical Reports
    9. Articles
    10. New Syndromes
    11. Letter to the Editor
    1. Fetal growth retardation, hydrocephalus, hypoplastic multilobed lungs, and other anomalies in 4 sibs (pages 276–279)

      K. Game, Dr. J. M. Friedman, B. Paradice and M. G. Norman

      Article first published online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320330226

  10. Letter to the Editor

    1. Top of page
    2. Masthead
    3. Articles
    4. New Syndromes
    5. Articles
    6. Brief Clinical Reports
    7. Articles
    8. Brief Clinical Reports
    9. Articles
    10. New Syndromes
    11. Letter to the Editor
    1. Immunodeficiency associated with Dandy–Walker-like malformation, congenital heart defect, and craniofacial abnormalities (pages 280–281)

      Roger Lauener, Reinhard Seger, Walter Jörg, Françoise Hallé, Regula Aeppli and Albert Schinzel

      Article first published online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320330227

    2. IVIC syndrome: Report of a third family (pages 282–283)

      A. Czeizel, P. Göblyös and I. Kodaj

      Article first published online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320330228

    3. Re: IVIC syndrome report by Czeizel et al (page 284)

      Giovanni Neri and Vincenza Sammito

      Article first published online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320330229

    4. Duplicate report crossing over in Norrie disease family (page 286)

      Julielani Ngo, M. Anne Spence, Victoria Cortessis, J. Bronwyn Bateman and Robert S. Sparkes

      Article first published online: 5 JUN 2005 | DOI: 10.1002/ajmg.1320330231

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