X-linked mixed deafness (DFN3): cloning and characterization of the critical region allows the identification of novel microdeletions-Reference-Cited by-同舟云学术

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X-linked mixed deafness (DFN3): cloning and characterization of the critical region allows the identification of novel microdeletions

Published:1994 Issue:7 Volume:3 Page:1151-1154
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:Hum Mol Genet

Author:

Huber Irene,Bitner-Gllndzicz Maria,de Kok Yvette J.M.,van der Maarel Silvère M.,Ishikawa-Brush Yumiko,Monaco Anthony P.,Robinson David,Malcolm Susan,Pembrey Marcus E.,Brunner Han G.,Cremers Frans P.M.,Ropers Hans-Hilger

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/3/7/1151/2446529/3-7-1151.pdf

Cited by 32 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 CNV Catalogue;Human Chromosome Variation: Heteromorphism, Polymorphism and Pathogenesis;2017

2. Pou3f4-Mediated Regulation of Ephrin-B2 Controls Temporal Bone Development in the Mouse;PLoS ONE;2014-10-09

3. Audiological and surgical evidence for the presence of a third window effect for the conductive hearing loss in DFNX2 deafness irrespective of types of mutations;European Archives of Oto-Rhino-Laryngology;2013-02-12

4. Clinical evaluation of DFN3 patients with deletions in the POU3F4 locus and detection of carrier female using MLPA;Clinical Genetics;2010-11-02

5. Positional Cloning of Deafness Genes;Methods in Molecular Biology;2009

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