Intrauterine phenotypic features associated with 16p11.2 recurrent microdeletions-Reference-Cited by-同舟云学术

Intrauterine phenotypic features associated with 16p11.2 recurrent microdeletions

Published:2018-03-30 Issue:6 Volume:38 Page:381-389
ISSN:0197-3851
Container-title:Prenatal Diagnosis
language:en
Short-container-title:Prenatal Diagnosis

Author:

Lin Shaobin¹^ORCID,Shi Shanshan²,Zhou Yi¹,Ji Yuanjun¹,Huang Peizhi¹,Wu Jianzhu¹,Chen Baojiang¹,Luo Yanmin¹^ORCID

Affiliation:

1. Fetal Medicine Center, Department of Obstetrics and Gynecology; The First Affiliated Hospital, Sun Yat-sen University; Guangzhou People's Republic of China

2. Fetal Medicine Center; The First Affiliated Hospital, Jinan University; Guangzhou People's Republic of China

Publisher

Wiley

Subject

Genetics (clinical),Obstetrics and Gynecology

Reference43 articles.

1. A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disorders;Zufferey;J Med Genet,2012

2. Association between microdeletion and microduplication at 16p11.2 and autism;Weiss;N Engl J Med,2008

3. CNVs conferring risk of autism or schizophrenia affect cognition in controls;Stefansson;Nature,2014

4. Structural variation of chromosomes in autism spectrum disorder;Marshall;Am J Hum Genet,2008

5. Recurrent 16p11.2 microdeletions in autism;Kumar;Hum Mol Genet,2008

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