Craniosynostosis in a patient with a de novo 15q15-q22 deletion-Reference-Cited by-同舟云学术

Craniosynostosis in a patient with a de novo 15q15-q22 deletion

Published:2008 Issue:11 Volume:146A Page:1462-1465
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Hiraki Yoko,Moriuchi Miyuki,Okamoto Nobuhiko,Ishikawa Nobutsune,Sugimoto Yosuke,Eguchi Kuniki,Sakai Haruya,Saitsu Hirotomo,Mizuguchi Takeshi,Harada Naoki,Matsumoto Naomichi

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference19 articles.

1. FBN1,TGFBR1, and the Marfan-craniosynostosis/mental retardation disorders revisited

2. Clinical features in a de novo interstitial deletion 15q13 to q15

3. Interstitial deletion of chromosome 15: two cases

4. Craniosynostosis in an infant with an interstitial deletion of 15q [46, XY,del(15)(q15q22.1)]

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