Clinical Genetics

Cover image for Clinical Genetics

March 1986

Volume 29, Issue 3

Pages 191–268

  1. Original Article

    1. Top of page
    2. Original Article
    3. Short Communication
    4. Letter to the Editor
    5. Announcement
    1. Genetic control over fragile X chromosome expression (pages 191–195)

      Frederick Hecht, Jean Pierre Fryns, Robert F. Vlietinck and Herman Van Den Berghe

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1986.tb00811.x

    2. Determination of cholinesterase and acetylcholinesterase in amniotic fluid : Uses in prenatal diagnosis and quality control (pages 196–203)

      B. Rafael Elejalde, Gregory Peck and Maria Mercedes de Elejalde

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1986.tb00812.x

    3. Usefulness of a registry of congenital malformations for genetic counseling and prenatal diagnosis (pages 204–210)

      C. Stoll, M-P. Roth, B. Dott and P. Bigel

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1986.tb00813.x

    4. α1-antitiypsin deficiency and the flaccid lung syndrome : The heterozygote controversy (pages 211–215)

      E. C. Klasen, I. Biemond and C. D. Laros

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1986.tb00814.x

    5. Number of loci responsible for the inheritance of high and low activity of paraoxonase (pages 216–221)

      Arne Nielsen, Hans Eiberg and Jan Mohr

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1986.tb00815.x

    6. The Cowden syndrome: a clinical and genetic study in 21 patients (pages 222–233)

      Th. M. Starink, J. P. W. van der Veen, F. Arwert, L. P. de Waal, G. G.de Lange, J. J. P. Gille and A. W. Eriksson

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1986.tb00816.x

    7. Proximal duplications of chromosome 15: clinical dilemmas (pages 234–240)

      O. J. Hood, Bobbye M. Rouse, L. H. Lockhart and J. B. Bodensteiner

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1986.tb00817.x

    8. Familial transmission of a non-Robertsonian translocation dicentric (pages 246–250)

      P. J. Howard and A. C. Berry

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1986.tb00819.x

    9. Homozygosity for a Y/22 chromosome translocation: t(Y;22) (q12;p12/13) (pages 251–257)

      N. J. Leschot, J. V.D. Velden, A. Marinkovic-Ilsen, S. M. Darling and L. E. Nijenhuis

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1986.tb00820.x

  2. Short Communication

    1. Top of page
    2. Original Article
    3. Short Communication
    4. Letter to the Editor
    5. Announcement
    1. Copper-measurement in a muscle-biopsy. A possible method for postmortem diagnosis of Menkes disease (pages 258–261)

      T. TØNNESEN, G. Müller-Schauenburg, E. Damsgaard and N. Horn

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1986.tb00821.x

  3. Letter to the Editor

    1. Top of page
    2. Original Article
    3. Short Communication
    4. Letter to the Editor
    5. Announcement
    1. Osteoporosis-pseudoglioma syndrome and the ocular form of osteogenesis imperfecta (page 262)

      M. Frontali and B. Dallapiccola

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1986.tb00822.x

    2. Osteoporosis-pseudoglioma syndrome (page 263)

      Professor Peter Beighton

      Version of Record online: 23 APR 2008 | DOI: 10.1111/j.1399-0004.1986.tb00823.x

  4. Announcement

    1. Top of page
    2. Original Article
    3. Short Communication
    4. Letter to the Editor
    5. Announcement

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