Clinical Genetics

Cover image for Clinical Genetics

March 1974

Volume 5, Issue 3

Pages 177–270

  1. Original Article

    1. Top of page
    2. Original Article
    1. Genetic counseling: an appraisal (pages 177–187)

      Beverly Dev. Reynolds, Mary H. Puck and Arthur Robinson

      Article first published online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1974.tb01680.x

    2. A woman with multiple congenital anomalies, mental retardation and mosaicism for an unusual translocation chromosome t (6;19) (pages 188–195)

      P. D. Pallister, K. Patau, S. L. Inhorn and J. M. Opitz

      Article first published online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1974.tb01681.x

    3. Cerebellar ataxia and total albinism: A kindred suggesting pleiotropism or linkage (pages 196–204)

      H. Skre and K. Berg

      Article first published online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1974.tb01682.x

    4. Incidence of chromosome aberrations in a child psychiatric hospital (pages 205–210)

      K. R. Christensen and J. Nielsen

      Article first published online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1974.tb01683.x

    5. X/XY mosaicism with short Y (pages 211–217)

      R. Berger, J. P. Relier, Ch. Salmon and A. Minkowski

      Article first published online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1974.tb01684.x

    6. Partial trisomy 13 in a case of Cyclopia with 13/14 translocation (pages 218–222)

      D. N. Singh, R. A. Wiscovitch, R. A. Osborne and G. R. Hennigar

      Article first published online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1974.tb01685.x

    7. The genetic entity of hypochondroplasia (pages 223–229)

      M. Frydman, M. Hertz and R. M. Goodman

      Article first published online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1974.tb01686.x

    8. Muscle histology in fetuses at risk for Duchenne muscular dystrophy (pages 230–233)

      James Toop and Alan E. H. Emery

      Article first published online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1974.tb01687.x

    9. Idiopathic haemochromatosis: An autosomal recessive disease (pages 234–241)

      R. Saddi and J. Feingold

      Article first published online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1974.tb01688.x

    10. Idiopathic haemochromatosis and diabetes mellitus (pages 242–247)

      R. Saddi and J. Feinoold

      Article first published online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1974.tb01689.x

    11. The relation of the sex of choreic and rigid subjects to the age at onset of Huntington's disease (pages 248–253)

      C. J. Brackenridge and M. Chamberlin

      Article first published online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1974.tb01690.x

    12. Case report of an extra, small, acrocentric chromosome in a non-mongoloid girl (pages 254–258)

      Kurt Kaijser

      Article first published online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1974.tb01691.x

    13. Patient with Down's syndrome and male pseudohermaphroditism with a 47, XY, +21/46, X, +21 karyotype (pages 259–262)

      R. Santos Mello, O. A. Souza, E. M. K. Sz Santos Mello and E. C. Pimentel

      Article first published online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1974.tb01692.x

    14. An infant with an XXXYY karyotype (pages 263–270)

      F. A. Lecluse- Van der Bilt, A. Hagemeijer, E. M. E. Smit, H. K. A. Visser and G. J. Vaandrager

      Article first published online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1974.tb01693.x

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