8q21.11 microdeletion in two patients with syndromic peters anomaly-Reference-Cited by-同舟云学术

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8q21.11 microdeletion in two patients with syndromic peters anomaly

Published:2016-07-05 Issue:9 Volume:170 Page:2471-2475
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Happ Hannah¹,Schilter Kala F.¹²,Weh Eric¹,Reis Linda M.¹,Semina Elena V.¹²³

Affiliation:

1. Department of Pediatrics and Children's Research Institute; Medical College of Wisconsin; Milwaukee Wisconsin

2. Department of Cell Biology, Neurobiology and Anatomy; Medical College of Wisconsin; Milwaukee Wisconsin

3. Department of Ophthalmology; Medical College of Wisconsin; Milwaukee Wisconsin

Funder

National Institutes of Health awards

Children's Hospital of Wisconsin

National Institutes of Health

Clinical and Translational Science Award (CTSA) program

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference23 articles.

1. Peters anomaly: Review of the literature;Bhandari;Cornea,2011

2. Integrated miRNA and mRNA expression profiling of tension force-induced bone formation in periodontal ligament cells;Chang;In Vitro Cell Dev Biol Anim,2015

3. ZFHX4 interacts with the NuRD core member CHD4 and regulates the glioblastoma tumor-initiating cell state;Chudnovsky;Cell Rep,2014

4. Accurate and objective copy number profiling using real-time quantitative PCR;D'haene;Methods,2010

5. A homeodomain-zinc finger protein, ZFHX4, is expressed in neuronal differentiation manner and suppressed in muscle differentiation manner;Hemmi;Biol Pharm Bull,2006

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1. Congenital anterior segment ocular disorders: Genotype-phenotype correlations and emerging novel mechanisms;Progress in Retinal and Eye Research;2024-09

2. Loss-of-function of the Zinc Finger Homeobox 4 (ZFHX4) gene underlies a neurodevelopmental disorder;2024-08-08

3. Anterior segment dysgenesis: part II—genetics and pathogenesis;Expert Review of Ophthalmology;2024-03-05

4. Ocular Manifestations of Peters Plus-Like Syndrome in 8q21.11 Microdeletion Syndrome;Cornea;2023-04-06

5. Congenital corneal staphyloma in 8q21.11 microdeletion syndrome;Ophthalmic Genetics;2022-11-07

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