The genetic bases for non-syndromic hearing loss among Chinese-Reference-Cited by-同舟云学术

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The genetic bases for non-syndromic hearing loss among Chinese

Published:2009-02-06 Issue:3 Volume:54 Page:131-140
ISSN:1434-5161
Container-title:Journal of Human Genetics
language:en
Short-container-title:J Hum Genet

Author:

Ouyang Xiao Mei,Yan Denise,Yuan Hui Jun,Pu Dai,Du Li Lin,Han Don Yi,Liu Xue Zhong

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://www.nature.com/articles/jhg20094.pdf

Reference153 articles.

1. Fraser, G. R. The Causes of Profound Deafness in Childhood (Johns Hopkins University Press: Baltimore, 1976).

2. Morton, N. E. Genetic epidemiology of hearing impairment. Ann. N. Y. Acad. Sci. 630, 16–31 (1991).

3. Marazita, M. L., Ploughman, L. M., Rawlings, B., Remington, E. & Nance, W. E. Genetic epidemiological studies of early-onset deafness in the US school-age population. Am. J. Med. Genet. 46, 486–491 (1993).

4. ACMG. Genetics evaluation guidelines for the etiologic diagnosis of congenital hearing loss. Genetic Evaluation of Congenital Hearing Loss Expert Panel: ACMG statement. Genet Med. 4, 162–171 (2002).

5. Hone, S. W. & Smith, R. J. Medical evaluation of pediatric hearing loss: laboratory, radiographic, and genetic testing. Otolaryngol. Clin. North Am. 35, 751–764 (2002).

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2. Targeted Linked-Read Sequencing for Direct Haplotype Phasing of Parental GJB2/SLC26A4 Alleles;The Journal of Molecular Diagnostics;2024-07

3. Hereditary deafness carrier screening in 9,993 Chinese individuals;Frontiers in Genetics;2024-01-11

4. Analysis of deafness susceptibility gene of neonates in northern Guangdong, China;Scientific Reports;2024-01-03

5. Targeted linked-read sequencing for direct haplotype phasing of parental GJB2/SLC26A4 alleles: A universal and dependable noninvasive prenatal diagnosis method applied to autosomal recessive nonsyndromic hearing loss in at-risk families;2022-12-05

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