A Novel Class of Pseudoautosomal Region 1 Deletions Downstream of SHOX Is Associated with Léri-Weill Dyschondrosteosis-Reference-Cited by-同舟云学术

A Novel Class of Pseudoautosomal Region 1 Deletions Downstream of SHOX Is Associated with Léri-Weill Dyschondrosteosis

Published:2005-10 Issue:4 Volume:77 Page:533-544
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Benito-Sanz Sara,Thomas N. Simon,Huber Céline,del Blanco Darya Gorbenko,Aza-Carmona Miriam,Crolla John A.,Maloney Vivienne,Argente Jesús,Campos-Barros Ángel,Cormier-Daire Valérie,Heath Karen E.

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference26 articles.

1. SHOX mutations in dyschondrosteosis (Léri-Weill syndrome);Belin;Nat Genet,1998

2. Tandem repeats finder: a program to analyze DNA sequences;Benson;Nucleic Acids Res,1999

3. Identification of short stature caused by SHOX defects and therapeutic effect of recombinant human growth hormone;Binder;J Clin Endocrinol Metab,2000

4. Transcriptional and translational regulation of the Léri-Weill and Turner syndrome homeobox gene SHOX;Blaschke;J Biol Chem,2003

5. The short stature homeobox gene SHOX is involved in skeletal abnormalities in Turner syndrome;Clement-Jones;Hum Mol Genet,2000

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