Clinical Genetics

Cover image for Clinical Genetics

September 1980

Volume 18, Issue 3

Pages 153–232

  1. Original Article

    1. Top of page
    2. Original Article
    3. Announcements
    1. Guadalajara camptodactyly syndrome : A distinct probably autosomal recessive disorder (pages 153–159)

      J. M. Cantú, H. Rivera, Z. Nazará, Q. Rojas, A. Hernández and D. García-Cruz

      Article first published online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1980.tb00863.x

    2. Genetic susceptibility to multiple sclerosis: a linkage analysis with age-of-onset corrections (pages 160–167)

      R. W. Haile, S. E. Hodge, B. R. Visscher, M. A. Spence, R. Detels, T. L. McAuliffe, M. S. Park and J. P. Dudley

      Article first published online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1980.tb00864.x

    3. Genetic counselling for adult polycystic kidney disease. Ultrasound a useful tool in pre-symptomatic diagnosis? (pages 168–172)

      BarendL. Hogewind, JanJ. Veltkamp, CornelisW. Koch and Jaap de Graeff

      Article first published online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1980.tb00865.x

    4. Familial Williams Syndrome (pages 173–176)

      X. Cortada, K. Taysi and A. F. Hartmann

      Article first published online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1980.tb00866.x

    5. Pitfalls in the prenatal diagnosis of propionic acidemia (pages 177–183)

      P. D. Buchanan, S. G. Kahler, L. Sweetman and W. L. Nyhan

      Article first published online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1980.tb00867.x

    6. Chlorpropamide-alcohol flushing is not useful for individual genetic counseling of diabetic patients (pages 189–190)

      M. Dreyer, J. Kühnau and H. W. Rüdiger

      Article first published online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1980.tb00869.x

    7. Familial occurrence of intracranial arterial occlusive disease (Moyamoya) in neurofibromatosis (pages 191–196)

      RobertP. ERICKSON, James Woolliscroft and RichardJ. Allen

      Article first published online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1980.tb00870.x

    8. HLA typing of cultured amniotic cells for the prenatal diagnosis of complement C4 deficiency (pages 197–200)

      MarilynS. Pollack, HansD. Ochs and Bo Dupont

      Article first published online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1980.tb00871.x

    9. Prior abortions and neural tube defects (pages 201–202)

      T. J. David, P. A. Townley and AmandaR. Goldstein

      Article first published online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1980.tb00872.x

    10. Sialidosis type 2 (acid neuraminidase deficiency): clinical and biochemical features of a further case (pages 203–210)

      RobinM. Winter, DallasM. Swallow, Michael Baraitser and Paul Purkiss

      Article first published online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1980.tb00873.x

    11. Dominantly inherited macular degeneration (Best's disease) in a homozygous father with 11 children (pages 211–216)

      S. Nordström and W. Thorburn

      Article first published online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1980.tb00874.x

    12. Prenatal detection of intestinal obstruction: deficient amniotic fluid disaccharidases in affected fetuses (pages 217–222)

      P. R. Morin, M. Potier, L. Dallaire, S. B. Melançon and A. Milunsky

      Article first published online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1980.tb00875.x

    13. Abnormalities of sexual differentiation in campomelic dwarfs (pages 223–225)

      R. M. Pauli and R. A. Pagon

      Article first published online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1980.tb00876.x

  2. Announcements

    1. Top of page
    2. Original Article
    3. Announcements
    1. Announcements (page 232)

      Article first published online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1980.tb00878.x

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