2q31.1 microdeletion syndrome: redefining the associated clinical phenotype-Reference-Cited by-同舟云学术

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2q31.1 microdeletion syndrome: redefining the associated clinical phenotype

Published:2010-11-10 Issue:2 Volume:48 Page:98-104
ISSN:0022-2593
Container-title:Journal of Medical Genetics
language:en
Short-container-title:Journal of Medical Genetics

Author:

Dimitrov B.,Balikova I.,de Ravel T.,Van Esch H.,De Smedt M.,Baten E.,Vermeesch J. R.,Bradinova I.,Simeonov E.,Devriendt K.,Fryns J.-P.,Debeer P.

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Cited by 29 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Genetics of Common Birth Defects in Newborns;Principles of Neonatology;2024

2. Three‐dimensional genome structure and function;MedComm;2023-07-08

3. Description of Copy Number Variations in a Series of Children and Adolescents with FASD in Reunion Island;Children;2023-04-07

4. Genetic cold cases: lessons from solving complex congenital limb disorders;Genes & Development;2023-03-29

5. 2q31 microdeletion syndrome with the velocardiofacial phenotype and review of the literature: a case report;2023-01-03

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