Clinical Genetics

Cover image for Clinical Genetics

September 1979

Volume 16, Issue 3

Pages 137–215

  1. Original Article

    1. Top of page
    2. Original Article
    3. Announcements
    1. Prenatal diagnosis of xeroderma pigmentosum (group C) using assays of unscheduled DNA synthesis and postreplication repair (pages 137–146)

      D. J. J. Halley, W. Keijzer, N. G. J. Jaspers, M. F. Niermeuer, W. J. Rleijer, J. Boué, A. Boué and D. Bootsma

      Article first published online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1979.tb00982.x

    2. Prader-Willi syndrome and chromosomal mosaicism 46, XY/47, XY, + mar in two cases (pages 147–150)

      Kim Fleischer Michaelsen, Claes Lundsteen and Flemming Juul Hansen

      Article first published online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1979.tb00983.x

    3. Complex de novo rearrangement of chromosome 9 with clinical features of monosomy 9p syndrome (pages 151–155)

      J. J. Hoo, M. I. Parslow, R. L. Shaw and A. M. O. Veale

      Article first published online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1979.tb00984.x

    4. Translocation 46XY, t (17;18) (q25;q21) in a mentally retarded boy with progressive eye abnormalities (pages 156–162)

      Arabella Smith, Verne Caradus and J. Graham Henry

      Article first published online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1979.tb00985.x

    5. Features of trisomy 18 and 18p-syndromes in an infant with 46, XY, i(18q) (pages 163–168)

      Harold N. Bass, Robert S. Sparkes and Alvin A. Miller

      Article first published online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1979.tb00986.x

    6. Oculodento-osseous dysplasia: heterogeneity or variable expression? (pages 169–177)

      P. Brighton, H. Hamersma and M. Raad

      Article first published online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1979.tb00987.x

    7. Two abnormal clones in the bone marrow cells of a patient with paroxysmal nocturnal hemoglobinuria (pages 178–182)

      A. M. Cohen, F. Shabtai, U. Lewinski, B. Klein and M. Djaldetti

      Article first published online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1979.tb00988.x

    8. Discovery of an inherited bisatellited metacentric microchromosome in amniotic cell culture (pages 183–190)

      D. R. Romavn, L. Columbano-GReen, R. H. Smythe and P. C. Dukes

      Article first published online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1979.tb00989.x

    9. A chromosome survey of a hospital for the mentally subnormal (pages 191–204)

      M. J. W. Faed, I. Robertson, M. A. S. Field and J. P. Mellon

      Article first published online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1979.tb00990.x

    10. Five familial cases with a trisomy 16p syndrome due to translocation (pages 205–214)

      N. J. Leschot, J. J. De Nef, J. P. M. Geraedts, M. J. Becker-Bloemkolk, A. Talma, J. B. Bijlsma and M. Verjaal

      Article first published online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1979.tb00991.x

  2. Announcements

    1. Top of page
    2. Original Article
    3. Announcements
    1. International Symposium (page 215)

      Article first published online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1979.tb00993.x

    2. The Japanese Society of Human Genetics (page 215)

      Article first published online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1979.tb00992.x

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