Clinical Genetics

Cover image for Clinical Genetics

September 1992

Volume 42, Issue 3

Pages 105–160

  1. Original Article

    1. Top of page
    2. Original Article
    3. Rapid Communication
    4. Letter to the Editor
    1. Putative monosomy 21 in two patients: clinical findings and investigation using fluorescence in situ hybridization (pages 105–109)

      Denis L. Viljoen, Frank Speleman, Ronald Smart, Nadine Van Roy, Joan du Toit and Jules Leroy

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1992.tb03219.x

    2. Prevalence of retinitis pigmentosa in Slovenia (pages 122–123)

      B. Peterlin, N. Cankl-Klain, V. Morela, B. Stirn, S. Rainer and V. Cerar

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1992.tb03222.x

    3. Reassessment of a chromosome 12q + marker by fluorescent in situ hybridization (FISH) (pages 124–128)

      A. Jaziorowska, G. E. Houck Jr., X.-L. Yao, S. L. Sklower-Brooks, K. E. Wisniewski, E. C. Jenkins and H. M. Wisniewski

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1992.tb03223.x

    4. Pseudohypoparathyroidism type I and Albright's hereditary osteodystrophy with a proximal 15q chromosomal deletion in mother and daughter (pages 129–134)

      Hans Hedeland, Kerstin Berntorp, Kristina Arheden and Ulf Kristoffersson

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1992.tb03224.x

    5. Cleft palate and complex chromosome rearrangements (pages 135–142)

      Boris G. Kousseff, Peter Papenhausen, Richard L. Neu, Yau-Ping Essig and Carmelo A. Saraceno

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1992.tb03225.x

    6. Reproductive behaviour following spontaneous loss of a pregnancy after prenatal diagnosis (pages 149–151)

      Helen Brandenburg, Jolanda Groenhuijzen, Milena G. J. Jahoda, Theo Stijnen, Maria A. J. de Ridder, Eva S. Sachs and Juriy W. Wladimiroff

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1992.tb03227.x

    7. Autosomal recessive microcephaly with early onset seizures and spasticity (pages 152–155)

      M. Silengo, M. Lerone, M. Martinelli, G. Martucciello, P. E. Caffarena, V. Jasonni and G. Romeo

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1992.tb03228.x

  2. Rapid Communication

    1. Top of page
    2. Original Article
    3. Rapid Communication
    4. Letter to the Editor
    1. The gene for Best's macular dystrophy is located at 11q13 in a Swedish family (pages 156–159)

      Kristina Forsman, Caroline Graff, Stefan Nordström, Kent Johansson, Eleonora Westermark, Erik Lundgren, Karl-Henrik Gustavson, Claes Wadelius and Gösta Holmgren

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1992.tb03229.x

  3. Letter to the Editor

    1. Top of page
    2. Original Article
    3. Rapid Communication
    4. Letter to the Editor
    1. Enzyme deficiencies as the cause of hereditary nonspherocytic hemolytic anemia (page 160)

      A. Casado, Ma Casado, Ma R De la Torre, Ma E Lopéz-Fernandez and D. Carrascosa

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1992.tb03230.x

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