22q11.2 microduplication in a family with recurrent fetal congenital heart disease-Reference-Cited by-同舟云学术

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22q11.2 microduplication in a family with recurrent fetal congenital heart disease

Published:2011-07 Issue:4 Volume:54 Page:e433-e436
ISSN:1769-7212
Container-title:European Journal of Medical Genetics
language:en
Short-container-title:European Journal of Medical Genetics

Author:

Hu Ping,Ji Xiuqing,Yang Chi,Zhang Jingjing,Lin Ying,Cheng Jian,Ma Dingyuan,Cao Li,Yi Long,Xu Zhengfeng

Funder

National Natural Science Foundation of China

Natural Science Foundation of Jiangsu Province

Foundation of Nanjing Municipal Science and Technology Bureau

Foundation of Nanjing Municipal Public Health Bureau

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics,General Medicine

Reference12 articles.

1. A common molecular basis for rearrangement disorders on chromosome 22q11;Edelmann;Hum. Mol. Genet.,1999

2. Identification of familial and de novo microduplications of 22q11.21–q11.23 distal to the 22q11.21 microdeletion syndrome region;Coppinger;Hum. Mol. Genet.,2009

3. Microduplication 22q11.2: a new chromosomal syndrome;Portnoi;Eur. J. Med. Genet.,2009

4. Microduplication and triplication of 22q11.2: a highly variable syndrome;Yobb;Am. J. Hum. Genet.,2005

5. The intrafamilial variability of the 22q11.2 microduplication encompasses a spectrum from minor cognitive deficits to severe congenital anomalies;de La Rochebrochard;Am. J. Med. Genet. A,2006

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2. Chromosome 22q11 copy number variants and single ventricle CHD;Cardiology in the Young;2022-02-24

3. Prenatal phenotype of 22q11 micro-duplications: A systematic review and report on 12 new cases;European Journal of Medical Genetics;2022-02

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