American Journal of Medical Genetics

Cover image for American Journal of Medical Genetics

6 November 1995

Volume 59, Issue 2

Pages fmi–fmi, 131–270

Currently known as: American Journal of Medical Genetics Part A

  1. Masthead

    1. Top of page
    2. Masthead
    3. Genetic Drift
    4. Articles
    5. Brief Clinical Reports
    6. Articles
    7. Brief Clinical Reports
    8. Articles
    9. Living History — Autobiography
    10. Letters to the Editors
    11. Book Review
    12. Books Received
    1. Masthead (page fmi)

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320590201

  2. Genetic Drift

    1. Top of page
    2. Masthead
    3. Genetic Drift
    4. Articles
    5. Brief Clinical Reports
    6. Articles
    7. Brief Clinical Reports
    8. Articles
    9. Living History — Autobiography
    10. Letters to the Editors
    11. Book Review
    12. Books Received
    1. Whispered hints (pages 131–133)

      Robert G. Resta

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320590202

  3. Articles

    1. Top of page
    2. Masthead
    3. Genetic Drift
    4. Articles
    5. Brief Clinical Reports
    6. Articles
    7. Brief Clinical Reports
    8. Articles
    9. Living History — Autobiography
    10. Letters to the Editors
    11. Book Review
    12. Books Received
    1. Spondyloperipheral dysplasia (pages 139–142)

      G. Sorge, M. Ruggieri and R. S. Lachman

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320590204

    2. X-linked ichthyosis without STS deficiency: Clinical, genetical, and molecular studies (pages 143–148)

      Renato Robledo, Paola Melis, Erika Schillinger, Ida Casciano, Ivan Balazs, Antoniettina Rinaldi, Marcello Siniscalco and Giorgio Filippi

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320590205

    3. Reduced fecundity in male ALS gene-carriers (pages 149–153)

      W. G. Johnson, P. R. Lucek, S. Chatkupt, Y. Furman, A. Lustenberger and A. Lazzarini

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320590206

  4. Brief Clinical Reports

    1. Top of page
    2. Masthead
    3. Genetic Drift
    4. Articles
    5. Brief Clinical Reports
    6. Articles
    7. Brief Clinical Reports
    8. Articles
    9. Living History — Autobiography
    10. Letters to the Editors
    11. Book Review
    12. Books Received
    1. Sternal cleft: Case report and review of a series of nine patients (pages 154–156)

      Delphine Héron, Stanislas Lyonnet, Laurence Iserin, Arnold Munnich and Jean-Paul Padovani

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320590207

  5. Articles

    1. Top of page
    2. Masthead
    3. Genetic Drift
    4. Articles
    5. Brief Clinical Reports
    6. Articles
    7. Brief Clinical Reports
    8. Articles
    9. Living History — Autobiography
    10. Letters to the Editors
    11. Book Review
    12. Books Received
    1. Achondrogenesis type II with polydactyly (pages 157–160)

      Monica Rittler and Iêda M. Orioli

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320590208

    2. Physical findings in 21q22 deletion suggest critical region for 21q— phenotype in q22 (pages 161–163)

      Dr. Demetrios S. Theodoropoulos, Janet M. Cowan, Ellen R. Elias and Cynthia Cole

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320590209

    3. Hemifacial hyperplasia with meningeal involvement: A variant of proteus syndrome? (pages 164–167)

      Ushio Haramoto, Seiichiro Kobayashi and Kitaro Ohmori

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320590210

    4. X-linked myotubular myopathy: Clinical observations in ten additional cases (pages 168–173)

      Maries Joseph, G. Shashidhar Pai, Kenton R. Holden and Gail Herman

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320590211

    5. Duplication and loss of chromosome 21 in two children with Down syndrome and acute leukemia (pages 174–181)

      Peter K. Rogan, Pamelyn Close, Jean-Louis Blouin, James R. Seip, Lee Gannutz, Roger L. Ladda and Stylianos E. Antonarakis

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320590212

    6. Two craniosynostotic patients with 11q deletions, and review of 48 cases (pages 193–198)

      Amy Feldman Lewanda, Susan Morsey, Cheryl S. Reid and Dr. Ethylin Wang Jabs

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320590215

    7. Phenotypic differences among patients with Bardet-Biedl syndrome linked to three different chromosome loci (pages 199–203)

      Rivka Carmi, Khalil Elbedour, Edwin M. Stone and Val C. Sheffield

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320590216

    8. Autosomal dominant optic nerve colobomas, vesicoureteral reflux, and renal anomalies (pages 204–208)

      Lisa A. Schimmenti, Mary Ella Pierpont, Becky L. M. Carpenter, Clifford E. Kashtan, Max R. Johnson and William B. Dobyns

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320590217

    9. Effect of paternal age in achondroplasia, thanatophoric dysplasia, and osteogenesis imperfecta (pages 209–217)

      Prof. Iêda M. Orioli, Eduardo E. Castilla, Gioacchino Scarano and Pierpaolo Mastroiacovo

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320590218

    10. Infundibulopelvic stenosis, multicystic kidney, and calyectasis in a kindred: Clinical observations and genetic analysis (pages 218–224)

      Megumi Kobayashi, Bernard S. Kaplan, Richard D. Bellah, Maria Sartore, Eric Rappaport, Mark W. Steele, Elaine Mansfield, Paolo Gasparini, Saul Surrey and Paolo Fortina

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320590219

    11. Ag-NOR studies in a human lymphocyte culture: Are variants localized to specific chromosomes? (pages 225–228)

      Mustafa Ozen, Vicki L. Hopwood and Professor Sen Pathak

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320590220

    12. Distinct craniofacial syndrome of lagophthalmia and bilateral cleft lip and palate (pages 229–233)

      Shirley Korula, Libby Wilson and Janet Salomonson

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320590221

  6. Brief Clinical Reports

    1. Top of page
    2. Masthead
    3. Genetic Drift
    4. Articles
    5. Brief Clinical Reports
    6. Articles
    7. Brief Clinical Reports
    8. Articles
    9. Living History — Autobiography
    10. Letters to the Editors
    11. Book Review
    12. Books Received
  7. Articles

    1. Top of page
    2. Masthead
    3. Genetic Drift
    4. Articles
    5. Brief Clinical Reports
    6. Articles
    7. Brief Clinical Reports
    8. Articles
    9. Living History — Autobiography
    10. Letters to the Editors
    11. Book Review
    12. Books Received
    1. Variant of odontoonychodermal dysplasia? (pages 242–244)

      W. P. Arnold, M. A. W. Merkx and P. M. Steijlen

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320590224

    2. Arthur G. Steinberg: An appreciation (pages 245–249)

      F. Clarke Fraser, Trefor Jenkins, Alexander G. Bearn and John M. Opitz

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320590225

  8. Living History — Autobiography

    1. Top of page
    2. Masthead
    3. Genetic Drift
    4. Articles
    5. Brief Clinical Reports
    6. Articles
    7. Brief Clinical Reports
    8. Articles
    9. Living History — Autobiography
    10. Letters to the Editors
    11. Book Review
    12. Books Received
    1. Much ado about me (pages 250–262)

      Arthur G. Steinberg

      Version of Record online: 3 JUN 2005 | DOI: 10.1002/ajmg.1320590226

  9. Letters to the Editors

    1. Top of page
    2. Masthead
    3. Genetic Drift
    4. Articles
    5. Brief Clinical Reports
    6. Articles
    7. Brief Clinical Reports
    8. Articles
    9. Living History — Autobiography
    10. Letters to the Editors
    11. Book Review
    12. Books Received
    1. Possible homozygous Waardenburg syndrome in a fetus with exencephaly (pages 263–265)

      Dr. Ségolène Aymé and Nicole Philip

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320590227

    2. More deletions in the 5′ region than in the central region of the dystrophin gene were identified among filipino duchenne and becker muscular dystrophy patients (pages 266–267)

      Eva Malia Cutiongco, Carmencita D. Padilla, Kaori Takenaka, Yuko Yamasaki, Masafumi Matsuo and Hisahide Nishio

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320590228

  10. Book Review

    1. Top of page
    2. Masthead
    3. Genetic Drift
    4. Articles
    5. Brief Clinical Reports
    6. Articles
    7. Brief Clinical Reports
    8. Articles
    9. Living History — Autobiography
    10. Letters to the Editors
    11. Book Review
    12. Books Received
  11. Books Received

    1. Top of page
    2. Masthead
    3. Genetic Drift
    4. Articles
    5. Brief Clinical Reports
    6. Articles
    7. Brief Clinical Reports
    8. Articles
    9. Living History — Autobiography
    10. Letters to the Editors
    11. Book Review
    12. Books Received
    1. Books received (pages 269–270)

      Version of Record online: 7 JUN 2005 | DOI: 10.1002/ajmg.1320590230

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