The prevalence and expression of inherited connexin 26 mutations associated with nonsyndromic hearing loss in the Israeli population-Reference-Cited by-同舟云学术

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The prevalence and expression of inherited connexin 26 mutations associated with nonsyndromic hearing loss in the Israeli population

Published:2000-01-31 Issue:1 Volume:106 Page:50-57
ISSN:0340-6717
Container-title:Human Genetics
language:
Short-container-title:Human Genetics

Author:

Sobe T.,Vreugde S.,Shahin H.,Berlin M.,Davis N.,Kanaan M.,Yaron Y.,Orr-Urtreger A.,Frydman M.,Shohat M.,Avraham K.B.

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Cited by 139 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. Etiologic Diagnosis of Genetic Hearing Loss in an Ethnically Diverse Deafness Cohort;Audiology and Neurotology;2024-08-23

2. Audiological Phenotypes of Connexin Gene Mutation Patterns: A Glance at Different GJB2/GJB6 Gene Mutation Profiles;Children;2024-02-03

3. Prenatal Diagnosis and Pregnancy Termination in Jewish and Muslim Women with a Deaf Child in Israel;Children;2023-08-23

4. Molecular Genetic Study of the Causes of Nonsyndromic Sensorineural Hearing Loss in Patients from Georgia;Russian Journal of Genetics;2022-05

5. Age Estimate of GJB2-p.(Arg143Trp) Founder Variant in Hearing Impairment in Ghana, Suggests Multiple Independent Origins across Populations;Biology;2022-03-21

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