4q21 microdeletion in a patient with epilepsy and brain malformations-Reference-Cited by-同舟云学术

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4q21 microdeletion in a patient with epilepsy and brain malformations

Published:2015-04-02 Issue:6 Volume:167 Page:1409-1413
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Yano Sho¹²,McNamara Meredithe²,Halbach Sara³,Waggoner Darrel²³

Affiliation:

1. Section of Pediatric Neurology; Department of Pediatrics; University of Chicago Comer Children's Hospital; Chicago Illinios

2. Department of Pediatrics; University of Chicago Comer Children's Hospital; Chicago Illinios

3. Department of Human Genetics; University of Chicago; Chicago Illinios

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.36910/fullpdf

Reference16 articles.

1. Expanding the spectrum of microdeletion 4q21 syndrome: a partial phenotype with incomplete deletion of the minimal critical region and a new association with cleft palate and Pierre Robin sequence;Bhoj;Am J Med Genet A,2013

2. 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

3. Consistent chromosome abnormalities identify novel polymicrogyria loci in 1p36.3, 2p16.1-p23.1, 4q21.21-q22.1, 6q26-q27, and 21q2;Dobyns;Am J Med Genet A,2008

4. Microdeletion at 4q21.3 is associated with intellectual disability, dysmorphic facies, hypotonia, and short stature;Dukes-Rimsky;Am J Med Genet A,2011

5. A new interstitial deletion of 4q (q21. 1::q22.1);Fagan;J Med Genet,1989

Cited by 3 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. Clinical comparison between terminal and interstitial 4q deletion in two unrelated children;2022-10-10

2. A de novo deletion in a boy with cerebral palsy suggests a refined critical region for the 4q21.22 microdeletion syndrome;American Journal of Medical Genetics Part A;2017-04-03

3. A de novo microtriplication at 4q21.21-q21.22 in a patient with a vascular malignant hemangioma, elongated sigmoid colon, developmental delay, and absence of speech;American Journal of Medical Genetics Part A;2016-06-10

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