Frequency of Usher syndrome in two pediatric populations: Implications for genetic screening of deaf and hard of hearing children-Reference-Cited by-同舟云学术

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Frequency of Usher syndrome in two pediatric populations: Implications for genetic screening of deaf and hard of hearing children

Published:2010-08 Issue:8 Volume:12 Page:512-516
ISSN:1098-3600
Container-title:Genetics in Medicine
language:en
Short-container-title:Genetics in Medicine

Author:

Kimberling William J.,Hildebrand Michael S.,Shearer A. Eliot,Jensen Maren L.,Halder Jennifer A.,Trzupek Karmen,Cohn Edward S.,Weleber Richard G.,Stone Edwin M.,Smith Richard J.H.

Publisher

Elsevier BV

Subject

Genetics (clinical)

Reference41 articles.

Cited by 188 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 novel compound heterozygous variant of MYO7A in Usher syndrome type 1;Experimental Eye Research;2024-10

2. Long-Term Outcomes of Cochlear Implantation in Usher Syndrome;Ear & Hearing;2024-09-02

3. Clinical Utility of Multimodal Imaging to Assess Macular Changes in Usher Syndrome: A Transversal Study;2024-08-10

4. Coalition for Global Hearing Health Hearing Care Pathways Working Group: Guidelines for Clinical Guidance for Readiness and Development of Evidence-Based Early Hearing Detection and Intervention Programs;Ear & Hearing;2024-05-24

5. Usher syndrome: Genetic diagnosis and current therapeutic approaches;World Journal of Otorhinolaryngology;2024-01-19

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