Clinical Genetics

Cover image for Clinical Genetics

April 1979

Volume 15, Issue 4

Pages 289–368

  1. Original Article

    1. Top of page
    2. Original Article
    3. Announcement
    1. Platelet monoamine oxidase in a pedigree with schizophrenia: an interlaboratory project (pages 289–299)

      Anna–Lena Ask, Jan A. Böök, Thomas Heyden, Svante B. Ross, Christina Unge, Lennart Wetterberg, Samuel Eiduson and Kiyofumi Kobayashi

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1979.tb01737.x

    2. Analysis of family resemblance for lipids and lipoproteins (pages 300–306)

      Lennart Iselius

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1979.tb01738.x

    3. Hereditary hypoceruloplasminemia (pages 311–316)

      C. Q. Edwards, D. M. Williams and G. E. Cartwright

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1979.tb01740.x

    4. Chromosome 8 abnormalities as components of neoplastic and hematologic disorders (pages 317–326)

      Vincent M. Riccardi and Judy Foroason

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1979.tb01741.x

    5. Trisomy 13 in bone marrow cells in acute myelocytic leukemia and myelofibrosis (pages 327–331)

      Lillian Y. F. Hsu, Michael L. Greenberg, Simona Kohan and Ruth Wittman

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1979.tb01742.x

    6. Partial triplication and deletion of 13q: study of a family presenting with bilateral retinoblastomas (pages 332–345)

      Vincent M. Riccardi, Helen Mintz Hittner, Uta Francke, Susan Pippjn, Gerald P. Holmquist, Frank L. Kretzer and Robert Ferrell

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1979.tb01743.x

    7. Genetic studies in a family with inverted nipples (mammillae invertita) (pages 346–350)

      R. Shafir, B. Bonne–Tamir, S. Ashbel, H. Tsur and R. M. Goodman

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1979.tb01744.x

    8. Prenatal diagnosis of severe congenital malformations associated with elevated amniotic fluid alpha–feto protein (pages 351–355)

      J. CHEMKE, R. NlSANl, R. KASSIF, M. LANCET, R. BEISER and N. HURWITZ

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1979.tb01745.x

    9. Autosomal recessive spastic paraplegia: evidence for demyelination (pages 356–360)

      Henry Rothschild, Leo Happel, Donald Rampp and Earl Hackett

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1979.tb01746.x

    10. Bloom's Syndrome. VII. Progress report for 1978 (pages 361–367)

      James German, David Bloom and Eberhard Passarge

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1979.tb01747.x

  2. Announcement

    1. Top of page
    2. Original Article
    3. Announcement

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