Clinical Genetics

Cover image for Clinical Genetics

May 1992

Volume 41, Issue 5

Pages 225–280

  1. Original Article

    1. Top of page
    2. Original Article
    3. Case Report
    4. Letter to the Editor
    1. Isodicentric chromosome 18 in an abnormal infant using chromosome specific DNA probe (pages 225–228)

      Nagwa A. Maguld and Razwan Hablblan

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1992.tb03670.x

    2. Polymorphisms at the GLUT2 (β-cell/liver) glucose transporter gene and non-insulin-dependent diabetes mellitus (NIDDM): analysis in affected pedigree members (pages 229–234)

      Marco G. Baroni, Juan C. Alcolado, Paolo Pozzilli, Maria G. Cavallo, Shu-Ri Li and David J. Galton

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1992.tb03671.x

    3. GM1-gangliosidosis: tandem duplication within exon 3 of β-galactosidase gene in an infantile patient (pages 235–238)

      Akihiro Oshima, Kunihlro Yoshida, Asayo Ishlzaki, Michie Sbimmoto, Yuklko Fukuhara, Hltoshi Sakuraba and Yoshiynkl Suzuki

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1992.tb03672.x

    4. Effect of chorionic villus sampling on utilization of prenatal diagnosis in women of advanced maternal age (pages 239–242)

      Helen Brandenburg, Coon G. Gho, Milena G. J. Jahoda, Theo Stijnen, Hans Bakker and Jury W. WIadimlroff

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1992.tb03673.x

    5. Dominantly inherited microcephaly, short stature and normal intelligence (pages 248–251)

      Raoul C. M. Hannekam, Aat van Rhijn and F. A. M. Hannekam

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1992.tb03675.x

    6. Deletions, duplications and novel restriction fragment length polymorphism in Duchenne and Becker muscular dystrophies (pages 252–258)

      Y. L. Lau, G. Srlvastava, V. Wong, Y. T. Liu, F. C. S. He and C. Y. Yeung

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1992.tb03676.x

    7. Dosage analysis at the CSF1 and CSF1R loci in a new case of partial trisomy 5q (pages 259–262)

      M. Genuardi, R. Flamia, G. Palka, G. Parruti and G. Nsri

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1992.tb03677.x

    8. An additional patient with the 3C syndrome (pages 263–265)

      F. Gurrieri and G. Narl

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1992.tb03678.x

    9. Cri du chat syndrome due to meiotic recombination in a pericentric inversion 5 carrier (pages 266–269)

      Judy E. Chernos, S. Boatrice Fowlow and David M. Cox

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1992.tb03679.x

    10. Genetic recombination between malignant hyperthermia and calcium release channel in skeletal muscle (pages 270–272)

      T. Fagerlund, G. Islander, E. Ranklov, I. Harbltz, J. G. Hange, E. Mokleby and K. Barg

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1992.tb03680.x

  2. Case Report

    1. Top of page
    2. Original Article
    3. Case Report
    4. Letter to the Editor
    1. Lethal congenital erythroderma: a newly recognised genetic disorder (pages 273–277)

      J. P. H. Shield, M. R. Jndge, W. Reardon, M. Baraitsar, V. Nohria, M. Malons and J. I. Harper

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1992.tb03681.x

  3. Letter to the Editor

    1. Top of page
    2. Original Article
    3. Case Report
    4. Letter to the Editor
    1. Interstitial deletion of 17pl 1.2 with brain abnormalities (pages 278–280)

      Mitsuo Masuno MD., Jun-ichi Asano MD., Miwa Arai MD., Takashi Kuwahara MD. and Tadao Orii MD.

      Version of Record online: 28 JUN 2008 | DOI: 10.1111/j.1399-0004.1992.tb03682.x

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