Genetic testing for hearing loss in the United States should include deletion/duplication analysis for the deafness/infertility locus at 15q15.3-Reference-Cited by-同舟云学术

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Genetic testing for hearing loss in the United States should include deletion/duplication analysis for the deafness/infertility locus at 15q15.3

Published:2013 Issue:1 Volume:6 Page:19
ISSN:1755-8166
Container-title:Molecular Cytogenetics
language:en
Short-container-title:Mol Cytogenet

Author:

Hoppman Nicole,Aypar Umut,Brodersen Pamela,Brown Neil,Wilson Justin,Babovic-Vuksanovic Dusica

Publisher

Springer Science and Business Media LLC

Subject

Biochemistry (medical),Genetics (clinical),Genetics,Molecular Biology,Molecular Medicine,Biochemistry

Reference6 articles.

1. Newborn Hearing Screening — A Silent Revolution

2. Sensorineural deafness and male infertility: a contiguous gene deletion syndrome

3. CATSPER2, a human autosomal nonsyndromic male infertility gene

4. Congenital Dyserythropoietic Anemia Type I Is Caused by Mutations in Codanin-1

5. A homozygous deletion of a normal variation locus in a patient with hearing loss from non-consanguineous parents

Cited by 38 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. Unraveling the Genetic Basis of Combined Deafness and Male Infertility Phenotypes through High‐Throughput Sequencing in a Unique Cohort from South India;Advanced Genetics;2024-05-08

2. Advances in Genetics of Male Infertility;Current and Future Advances in Male Infertility;2024

3. Maximizing the Detection of Copy Number Variants in the Highly Homologous Deafness-Infertility Syndrome Locus in Standard-of-care Testing;Clinical Chemistry;2023-05-12

4. Leveraging Unique Chromosomal Microarray Probes to Accurately Detect Copy Number at the Highly Homologous 15q15.3 Deafness-Infertility Syndrome Locus;Clinical Chemistry;2023-04-06

5. Frequency of the STRC-CATSPER2 deletion in STRC-associated hearing loss patients;Scientific Reports;2022-01-12

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