Clinical Genetics

Cover image for Clinical Genetics

July 1981

Volume 20, Issue 1

Pages 1–78

  1. Original Article

    1. Top of page
    2. Original Article
    3. Letter to the Editors
    1. A new growth deficiency syndrome (pages 1–5)

      Selma A. Myhre, Rogelio H. A. Ruvalcaba and C. Benjamin Graham

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1981.tb01798.x

    2. Clinically manifesting carriers in Duchenne muscular dystrophy (pages 6–12)

      Mieko Yoshioka

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1981.tb01799.x

    3. Cleft palate: A genetic and epidemiologic investigation (pages 13–24)

      Edward D. Shields, David Bixler and Poul Fogh-Andersen

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1981.tb01800.x

    4. Dominant inheritance of microcephaly with short stature (pages 25–27)

      Barbara K. Burton

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1981.tb01801.x

    5. Gonadal dysgenesis, intra-X chromosome insertion, and possible position effect in an otherwise normal female (pages 28–35)

      Frank S. Grass, Robert P. Schwartz, Jane O. Deal and James C. Parke Jr

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1981.tb01802.x

    6. An Indian family with postaxial Polydactyly in four generations (pages 36–39)

      Kiran Kucheria, R. K. Kenue and Neelam Taneja

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1981.tb01803.x

    7. Familial 5/14 translocation with triple X and 47,XY + 14q- (pages 40–43)

      M. Lancet, L. Sindel and I. Segal

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1981.tb01804.x

    8. Polymorphism in chromosome 4 (pages 44–47)

      S. Bardhan, D. N. Singh and K. Davis

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1981.tb01805.x

    9. 46,XY/48,XXY,+8 in a male with clinical and dermatoglyphic features of mosaic trisomy 8 syndrome (pages 60–63)

      Pamela A. Casey, Constance E. Clark and Henry R. Cowell

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1981.tb01808.x

    10. Urinary amino acids and organic acids in the Sjögren-Larsson syndrome (pages 64–66)

      G. Holmgren, S. Jagell, H. Seeman and G. Steen

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1981.tb01809.x

    11. Adrenal adenomas in a patient with Gardner's syndrome (pages 67–73)

      Edwin W. Naylor and Eldon I. Gardner

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1981.tb01810.x

    12. Phenotypic variation in Meckel syndrome (pages 74–77)

      Mary J. Seller

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1981.tb01811.x

  2. Letter to the Editors

    1. Top of page
    2. Original Article
    3. Letter to the Editors
    1. “Fragile X” Chromosome in Normal Males (page 78)

      Patricia N. Howard-Peebles

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1981.tb01812.x

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