Literature DB >> 6331789

[Cri-du-chat syndrome and trisomy 8p due to a paternal translocation t(5;8)(p1409;p12)].

M O Rethoré, J Couturier, E Villain, M Hambourg, J Lejeune.   

Abstract

Cri du chat disease and trisomy 8p were observed in a male patient. His father was carrier of a balanced de novo t(5;8)(p1409p12).

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Year:  1984        PMID： 6331789

Source DB:  PubMed          Journal:  Ann Genet        ISSN： 0003-3995


  2 in total

1.  Trisomy 8p: unusual origin detected by fluorescence in situ hybridization.

Authors:  C M Moore; K Barnum; C I Kaye; K S Kagan-Hallett; J C Liang
Journal:  Hum Genet       Date:  1992-05       Impact factor: 4.132

Review 2.  Delineation of 14q32.3 deletion syndrome.

Authors:  A P Ortigas; C K Stein; L L Thomson; J J Hoo
Journal:  J Med Genet       Date:  1997-06       Impact factor: 6.318
  2 in total

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