Clinical Genetics

Cover image for Clinical Genetics

September 1993

Volume 44, Issue 3

Pages 113–167

  1. Original Article

    1. Top of page
    2. Original Article
    3. Short communication
    4. Letter to the Editor
    1. DNA polymorphisms of the apolipoprotein B gene are associated with obesity and serum lipids in healthy Indians in Singapore (pages 113–120)

      N. Saha, J. S. H. Tay, G. K. Heng and S. E. Humphries

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1993.tb03861.x

    2. Ambras syndrome: delineation of a unique hypertrichosis universalis congenita and association with a balanced pericentric inversion (8) (p11.2; q22) (pages 121–128)

      F. A. M. Baumeister, J. Egger, M. T. Schildhauer and S. Stengel-Rutkowski

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1993.tb03862.x

    3. Anthropometric and craniofacial patterns in mentally retarded males with emphasis on the fragile X syndrome (pages 129–138)

      Merlin G. Butler, Riccardo Pratesi, Michael S. Watson, W. Roy Breg and Dharmdeo N. Singh

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1993.tb03863.x

    4. Prenatal detection of an inverted X chromosome in a male (pages 139–141)

      Arthur R. Brothman, Anna Newlin, Susan E. Phillips, Gretchen Q. Kinzie and Lawrence G. Leichtman

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1993.tb03864.x

    5. Y chromosome mosaicism in the gonads, but not in the blood, of a girl with the Turner phenotype and virilized external genitalia (pages 142–145)

      Tarek Bisat, Kristin May, Stuart Litwer and Bruce Broecker

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1993.tb03865.x

    6. MCA/MR syndrome with features of Hallermann-Streiff syndrome and 4q deficiency/ 14q duplication (pages 146–148)

      J. P. Fryns, M. Borghgraef, F. Lemmens and H. van den Berghe

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1993.tb03866.x

    7. Further evidence for the location of the blepharophimosis syndrome (BPES) at 3q22.3-q23 (pages 149–151)

      J. P. Fryns, P. Stromme and H. van den Berghe

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1993.tb03867.x

    8. Progressive pseudorheumatoid arthritis of childhood (PPAC) and normal adult height (pages 152–155)

      E. Legius, M. Mulier, B. van Damme and J. P. Fryns

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1993.tb03868.x

    9. Molecular cytogenetic analysis of a familial pericentric inversion of chromosome 12 (pages 156–163)

      Frank Speleman, Nadine van Roy, Eric De Vos, Carl Hilliker, Ron F. S. Suijkerbuijk and Juies G. Leroy

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1993.tb03869.x

  2. Short communication

    1. Top of page
    2. Original Article
    3. Short communication
    4. Letter to the Editor
    1. Bilateral vocal cord paralysis in Williams syndrome (pages 164–165)

      F. J. Stewart, M. Dalzell, M. McReid and M. J. Cinnamond

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1993.tb03870.x

  3. Letter to the Editor

    1. Top of page
    2. Original Article
    3. Short communication
    4. Letter to the Editor
    1. Case of human chimerism detected by unbalanced chromosome translocation? (page 166)

      C. G. Woods and K. K. Smith

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1993.tb03871.x

    2. De novo DNA rearrangement in atypical facioscapulohumeral muscular dystrophy (page 167)

      P. Jardine, M. Jones, L. Tyfield, M. Upadhyaya and P. Lunt

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1993.tb03872.x

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