Xp21 deletion in female patients with intellectual disability: Two new cases and a review of the literature-Reference-Cited by-同舟云学术

Xp21 deletion in female patients with intellectual disability: Two new cases and a review of the literature

Published:2015-06 Issue:6-7 Volume:58 Page:341-345
ISSN:1769-7212
Container-title:European Journal of Medical Genetics
language:en
Short-container-title:European Journal of Medical Genetics

Author:

Heide Solveig^ORCID,Afenjar Alexandra,Edery Patrick,Sanlaville Damien,Keren Boris,Rouen Alexandre,Lavillaureix Alinoë,Hyon Capucine,Doummar Diane,Siffroi Jean-Pierre,Chantot-Bastaraud Sandra

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics,General Medicine

Reference25 articles.

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3. A dosage sensitive locus at chromosome Xp21 is involved in male to female sex reversal;Bardoni;Nat Genet,1994

4. Intragenic deletions of IL1RAPL1: report of two cases and review of the literature;Behnecke;Am J Med Genet A,2011

5. Molecular diagnosis of Duchenne/Becker muscular dystrophy: enhanced detection of dystrophin gene rearrangements by oligonucleotide array-comparative genomic hybridization;Del Gaudio;Hum Mutat,2008

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