A de novo 1.9-Mb interstitial deletion of 3q13.2q13.31 in a girl with dysmorphic features, muscle hypotonia, and developmental delay-Reference-Cited by-同舟云学术

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A de novo 1.9-Mb interstitial deletion of 3q13.2q13.31 in a girl with dysmorphic features, muscle hypotonia, and developmental delay

Published:2009-07-16 Issue:8 Volume:149A Page:1818-1822
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Shimojima Keiko,Saito Kayoko,Yamamoto Toshiyuki

Funder

Special Coordination Funds for Promoting Science and Technology, Ministry of Education, Culture, Sports, Science and Technology (Japan)

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.32963/fullpdf

Reference21 articles.

1. A targeted mutation of the D3 dopamine receptor gene is associated with hyperactivity in mice;Accili;Proc Natl Acad Sci USA,1996

2. A case report of partial deletion of the long arm of the No.3 chromosome;Arai;Med Genet Res,1982

3. Dopaminergic mechanism of reward-related incentive learning: Focus on the dopamine D(3) receptor;Beninger;Neurotox Res,2008

4. Boy with a chromosome del(3)(q12q23) and blepharophimosis syndrome;Fujita;Am J Med Genet,1992

5. A new case of interstitial deletion of chromosome 3q, del(3q)(q13.12q21.3), with agenesis of the corpus callosum;Genuardi;Clin Dysmorphol,1994

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