First reported case of interstitial 15 q15.3-q21.3 deletion diagnosed prenatally and characterized with array CGH in a fetus with an isolated short femur-Reference-Cited by-同舟云学术

First reported case of interstitial 15 q15.3-q21.3 deletion diagnosed prenatally and characterized with array CGH in a fetus with an isolated short femur

Published:2012-02-02 Issue:3 Volume:158A Page:617-621
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Abdelhedi Fatma,Corcos Johanna,Cuisset Laurence,Tsatsaris Vassilis,Tantau Julia,Le Tessier Dominique,Lebbar Aziza,Dupont Jean-Michel

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference8 articles.

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2. Craniosynostosis in a patient with a de novo 15q15-q22 deletion;Hiraki;Am J Med Genet Part A,2008

3. Allelic variation in normal human FBN1 expression in a family with Marfan syndrome: A potential modifier of phenotype;Hutchinson;Hum Mol Genet,2003

4. A de novo deletion of chromosome 15(q15.2q21.2) in a dysmorphic mentally retarded child with congenital scalp defect;Koivisto;Clin Dysmorphol,1999

5. Coarctation of the aorta and mild to moderate developmental delay in a child with a de novo deletion of chromosome 15(q21.JT1q22.2);Lalani;BMC Med Genet,2006

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