HOXA 2 Haploinsufficiency in Dominant Bilateral Microtia and Hearing Loss-Reference-Cited by-同舟云学术

HOXA 2 Haploinsufficiency in Dominant Bilateral Microtia and Hearing Loss

Published:2013-07-11 Issue:10 Volume:34 Page:1347-1351
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Human Mutation

Author:

Brown Kerry K.¹²,Viana Lucas M.¹³⁴,Helwig Cecilia C.⁵,Artunduaga Maria A.⁶,Quintanilla‐Dieck Lourdes⁷,Jarrin Patricia⁸,Osorno Gabriel⁹,McDonough Barbara¹²,DePalma Steven R.¹¹⁰,Eavey Roland D.¹¹,Seidman Jonathan G.¹,Seidman Christine E.¹²¹⁰

Affiliation:

1. Department of Genetics Harvard Medical School Boston Massachusetts

2. Cardiovascular Division Brigham and Women's Hospital Boston Massachusetts

3. Department of Otology and Laryngology Massachusetts Eye and Ear Infirmary Boston Massachusetts

4. Faculty of Health Sciences University of Brasilia Brasilia Brazil

5. Department of Pediatric Otolaryngology Geisinger Medical Center Danville Pennsylvania

6. Section of Plastic and Reconstructive Surgery Department of Surgery University of Chicago Medical Center Chicago Illinois

7. Department of Otolaryngology Head & Neck Surgery Oregon Health and Science University Portland Oregon

8. Sistema de Salud Integral Fundación Tierra Nueva Hospital Un Canto a la Vida Quito Ecuador

9. Unidad de Cirugía Plástica Facultad de Medicina Universidad Nacional de Colombia Bogotá Colombia

10. Howard Hughes Medical Institute

11. Department of Otolaryngology Vanderbilt Bill Wilkerson Center Vanderbilt University Medical Center Nashville Tennessee

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/humu.22367

Reference18 articles.

1. A human homologue of the Drosophila eyes absent gene underlies Branchio-Oto-Renal (BOR) syndrome and identifies a novel gene family

2. A Mutation in HOXA2 Is Responsible for Autosomal-Recessive Microtia in an Iranian Family

3. Epidemiologic features and clinical subgroups of anotia/microtia in Texas

4. A framework for variation discovery and genotyping using next-generation DNA sequencing data

5. Hoxa-2 mutant mice exhibit homeotic transformation of skeletal elements derived from cranial neural crest

Cited by 41 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. A multiple super-enhancer region establishes inter-TAD interactions and controls Hoxa function in cranial neural crest;Nature Communications;2023-06-05

2. The role of genetic factors in microtia: A systematic review;F1000Research;2023-04-26

3. Shaping faces: genetic and epigenetic control of craniofacial morphogenesis;Nature Reviews Genetics;2023-04-24

4. Development and Developmental Disorders of the Brain Stem;Clinical Neuroembryology;2023

5. The Enigmatic Etiology of Oculo-Auriculo-Vertebral Spectrum (OAVS): An Exploratory Gene Variant Interaction Approach in Candidate Genes;Life;2022-10-28