Genotype-phenotype analysis of the branchio-oculo-facial syndrome-Reference-Cited by-同舟云学术

Genotype-phenotype analysis of the branchio-oculo-facial syndrome

Published:2010-12-28 Issue:1 Volume:155 Page:22-32
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Milunsky Jeff M.,Maher Tom M.,Zhao Geping,Wang Zhenyuan,Mulliken John B.,Chitayat David,Clemens Michele,Stalker Heather J.,Bauer Mislen,Burch Michele,Chénier Sébastien,Cunningham Michael L.,Drack Arlene V.,Janssens Sandra,Karlea Audrey,Klatt Regan,Kini Usha,Klein Ophir,Lachmeijer Augusta M.,Megarbane Andre,Mendelsohn Nancy J.,Meschino Wendy S.,Mortier Geert R.,Parkash Sandhya,Ray C. Renai,Roberts Angharad,Roberts Amy,Reardon Willie,Schnur Rhonda E.,Smith Rosemarie,Splitt Miranda,Tezcan Kamer,Whiteford Margo L.,Wong Derek A.,Zori Roberto,Lin Angela E.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.33783/fullpdf

Reference23 articles.

1. Temporal bone anomaly proposed as a major criteria for diagnosis of CHARGE syndrome;Amiel;Am J Med Genet,2001

2. Branchio-oculo-facial syndrome with cleft lip and bilateral dermal thymus;Bennaceur;Cleft Palate Craniofac J,1998

3. Temporal bone anomalies in the branchio-oto-renal syndrome: Detailed computed tomographic and magnetic resonance imaging findings;Ceruti;Otol Neurotol,2002

4. Transcription factor AP-2 and monoaminergic functions in the central nervous system;Damberg;J Neural Transm,2005

5. An interstitial deletion of 6p24-p25 proximal to the FKHL7 locus and including AP-2α that affects anterior eye chamber development;Davies;J Med Genet,1999

Cited by 59 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. The heterogeneous genetic architectures of orofacial clefts;Trends in Genetics;2024-05

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

3. A neonatal case report of branchiooculofacial syndrome caused by a novel mutation in the TFAP2A gene and literature review;Medicine;2023-11-03

4. Auricular fistula: a review of its clinical manifestations, genetics, and treatments;Journal of Molecular Medicine;2023-07-17

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