Further defining the critical genes for the 4q21 microdeletion disorder-Reference-Cited by-同舟云学术

Further defining the critical genes for the 4q21 microdeletion disorder

Published:2016-09-08 Issue:1 Volume:173 Page:120-125
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Hu Xuyun¹²,Chen Xiaoli³,Wu Bingbing⁴,Soler Irene Mademont⁵,Chen Shaoke²,Shen Yiping¹²⁶

Affiliation:

1. Shanghai Children's Medical Center; Shanghai Jiao Tong University School of Medicine; Shanghai P.R. China

2. Genetic and Metabolic Central Laboratory; Guangxi Maternal and Child Health Hospital; Nanning Guangxi P.R. China

3. Municipal Key Laboratory of Child Development and Nutriomics; Capital Institute of Pediatrics; Beijing P.R. China

4. Molecular Genetic Diagnosis Center; Shanghai Key Lab of Birth Defects; Pediatrics Research Institute; Children's Hospital of Fudan University; Shanghai P.R. China

5. Cardiovascular Genetics Center; University of Girona-IdIBGi; Girona Spain

6. Departments of Laboratory Medicine and Pathology; Boston Children's Hospital; Harvard Medical School; Boston Massachusetts

Funder

Shanghai Science and Technology Commission

“Eastern Scholar” Fund

Natural Science Foundation of China

Advanced Personnel Training Program

Innovation Project of Beijing Municipal Human Resources

Social Security Bureau

Capital Health Research and Development

Publisher

Wiley

Subject

Genetics(clinical),Genetics

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4. Microdeletion at chromosome 4q21 defines a new emerging syndrome with marked growth restriction, mental retardation and absent or severely delayed speech;Bonnet;J Med Genet,2010

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