SHOX gene mutations and deletions in dyschondrosteosis or Leri-Weill syndrome-Reference-Cited by-同舟云学术

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SHOX gene mutations and deletions in dyschondrosteosis or Leri-Weill syndrome

Published:1999-12 Issue:s433 Volume:88 Page:55-59
ISSN:0803-5253
Container-title:Acta Paediatrica
language:en
Short-container-title:Acta Paediatrica

Author:

Cormier-Daire V,Belin V,Cusin V,Viot G,Girlich D,Toutain A,Moncla A,Vekemans M,Merrer M Le,Munnich A

Publisher

Wiley

Subject

General Medicine,Pediatrics, Perinatology, and Child Health

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1651-2227.1999.tb14404.x/fullpdf

Reference16 articles.

1. Sex-influenced expression of Madelung's deformity in a family of dyschondrosteosis.

2. Observations in a case of an X/Y translocation, t(X;Y)(p22;q11), in a mother and son

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