• Issue

    Clinical Genetics: Volume 39, Issue 2

    81-159
    February 1991
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Original Article

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The prevalence of chromosome diseases in the general population of Sichuan, China

Sizhong Zhang,  Tao Xie,  Yongcai Tang,  Silig Zhang,  Yin Xu, 
  • Pages: 81-88
  • First Published: February 1991
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Frequency of the phenylalanine deletion (ΔF508) in the CF gene of Belgian cystic fibrosis patients

Jan G. Wauters,  Jan Hendrickx,  Paul Coucke,  Lieve Vits,  Karel Stuer,  Lutgard van Schil,  Bart J. van der Auwera,  August Van Elsen,  Jan Dumon,  Patrick J. Willems, 
  • Pages: 89-92
  • First Published: February 1991
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Robertsonian translocation and an extra microchromosome: independent origin identified by in situ hybridization

A. C. Heppell-Parton,  J. J. Waters, 
  • Pages: 93-96
  • First Published: February 1991
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Routine applications of DNA fingerprinting with the oligonucleotide probe (CAC)5/(GTG)5

H. Neitzel,  M. Digweed,  P. Nürnberg,  A. Pöpperl,  C. A. Schmidt,  S. Tinschert,  K. Sperling, 
  • Pages: 97-103
  • First Published: February 1991
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The cerebro-reno-digital syndromes: a new community

I. W. Lurie,  G. I. Lazjuk,  I. A. Korotkova,  E. D. Cherstvoy, 
  • Pages: 104-113
  • First Published: February 1991
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Rapp-Hodgkin hypohidrotic ectodermal dysplasia syndrome

Ian R. Walpole,  Jack Goldblatt, 
  • Pages: 114-120
  • First Published: February 1991
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Using the polymerase chain reaction to maintain DNA probe inventories in clinical and diagnostic laboratories

Jack Tarleton,  Charles E. Schwartz, 
  • Pages: 121-124
  • First Published: February 1991
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Counselling under genetic heterogeneity: a practical approach

Steven Narod, 
  • Pages: 125-131
  • First Published: February 1991

Case Report

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Short arm deletion of chromosome 1: del(1)(p13.3 p22.3) in a female infant with an extreme tetralogy of Fallot

Hiroshi Tabata,  Katsuhiko Sone,  Toshihiro Kobayashi,  Takayuki Yanagisawa,  Tadahisa Tamura,  Nobuzou Shimizu,  Yuzuru Kanbe,  Masahiko Tashiro,  Sanayasu Ono,  Takayoshi Kuroume, 
  • Pages: 132-135
  • First Published: February 1991
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Brief clinical report: a 46,XY phenotypic female with Smith-Lemli-Opitz syndrome

Mary F. Lachman,  Yvonne Wright,  David A. H. Whiteman,  Victor Herson,  Robert M. Greenstein, 
  • Pages: 136-141
  • First Published: February 1991
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Trisomy 18 and 18p- features in a case of isochromosome 18q [46,XY,i(18q)]: prenatal diagnosis and autopsy report

Doris H. Wurster-Hill,  J. Miguel Marin-Padilla,  John B. Moeschler,  Jonathan P. Park,  Melanie McDermet, 
  • Pages: 142-148
  • First Published: February 1991
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Unstable translocations: a new case?

T. Mattina,  G. Milana,  A. D'Agata,  L. Conti,  F. Sciacca, 
  • Pages: 149-150
  • First Published: February 1991
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Ring chromosome 4 in a child with mild dysmorphic signs

Gabriele Freyberger,  Christine Wamsler,  Michael Schmid, 
  • Pages: 151-155
  • First Published: February 1991

Letter to the Editors

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XY translocation in a boy with ichthyosis, hypogonadism, short stature and mental retardation

T. Matsumoto,  K. Taku,  T. Miike,  N. Harada,  N. Niikawa, 
  • Pages: 156-158
  • First Published: February 1991

Announcement

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Annual Meeting of the European Society of Human Genetics

  • Page: 159
  • First Published: February 1991