Clinical Genetics

Cover image for Clinical Genetics

February 1976

Volume 9, Issue 2

Pages 113–254

  1. Original Article

    1. Top of page
    2. Original Article
    1. A 45, X woman with a 47, XY, G+ son (pages 113–116)

      Iwonna Lajborek-Czyź

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1976.tb01555.x

    2. Histidinuria: A renal and intestinal histidine transport deficiency found in two mentally retarded children (pages 117–124)

      Juan Sabater, Carmen Ferré, Maria Puliol and Antonio Maya

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1976.tb01556.x

    3. X-linked nonspecific mental retardation:Report of a large kindred (pages 125–130)

      Karen M. Yarbrough and Patricia N. Howard-Peebles

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1976.tb01557.x

    4. Red cell glucose-6-phosphate dehydrogenase deficiency in ethnic groups in Israel (pages 131–133)

      J. L. Zaidman, H. Leiba, S. Scharf and I. Steinman

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1976.tb01558.x

    5. Identical tetramelic monodactyly in two brothers (pages 143–148)

      Jirí Svejcar, Jürgen Kleinebrecht and Karl-Heinz Degenhardt

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1976.tb01560.x

    6. Further observations on familial hypobetaliproteinaemia (pages 149–155)

      I. Tamir, O. Levtow, D. Lotan, C. Legum, D. Heldenberg and B. Werbin

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1976.tb01561.x

    7. 48, XXXY Klinefelter syndrome and nail-patella syndrome in the same child (pages 163–168)

      Jette Jansen, Erik Hansen, Niels Hobolth, Petrea Jacobsen and Margareta Mikkelsen

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1976.tb01563.x

    8. Polycystic kidney disease in a patient with the oral-facial-digital syndrome-Type I (pages 183–186)

      M. J. E. Harrod, J. Stokes, L. F. Peede and J. L. Goldstein

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1976.tb01565.x

    9. A case of trisomy 20? (pages 187–191)

      Jan Wahlström, Jan Borsgård and Karl-Göran Sabel

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1976.tb01566.x

    10. An isochromosome of the short arms of the no. 18 chromosome in a mentally retarded girl (pages 192–196)

      Petr Balíĉek, Jan Zižka and Josef Lichý

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1976.tb01567.x

    11. Autosomal recessive muscular dystrophy in Manitoba Hutterites (pages 197–202)

      M. H. K. Shokeir and N. L. Kobrinsky

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1976.tb01568.x

    12. Cerebellar ataxia and hypergonadotropic hypogonadism in two kindreds. Chance concurrence, pleiotropism or linkage? (pages 234–244)

      Håvard Skre, Hans H. Bassöe, Kåre Berg and Arne G. Frövig

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1976.tb01570.x

    13. Inheritance of hypoplastic left heart syndrome (HLHS): Further observations (pages 245–249)

      L. G. Brownell and M. H. K. Shokeir

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1976.tb01571.x

    14. Partial trisomy of the long arm of chromosome 7 (pages 250–254)

      A. Al Saadi and Hassan A. Moghadam

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1976.tb01572.x

SEARCH

SEARCH BY CITATION