Genotype phenotype correlations for hearing impairment: Approaches to management-Reference-Cited by-同舟云学术

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Genotype phenotype correlations for hearing impairment: Approaches to management

Published:2014-02-18 Issue:6 Volume:85 Page:514-523
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:Clin Genet

Author:

Hoefsloot L. H.¹²,Feenstra I.¹²,Kunst H. P. M.³⁴,Kremer H.¹³⁴⁵

Affiliation:

1. Department of Human Genetics; Radboud University Medical Center; Nijmegen the Netherlands

2. Institute for Genetic and Metabolic Disease; Radboud University Medical Center; Nijmegen the Netherlands

3. Department of Otorhinolaryngology, Head and Neck Surgery; Radboud University Medical Center; Nijmegen the Netherlands

4. Donders Institute for Brain, Cognition and Behaviour; Radboud University Medical Center; Nijmegen the Netherlands

5. Nijmegen Center for Molecular Life Sciences; Radboud University Medical Center; Nijmegen the Netherlands

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference26 articles.

1. Prevalence of permanent childhood hearing impairment in the United Kingdom and implications for universal neonatal hearing screening: questionnaire based ascertainment study;Fortnum;BMJ,2001

2. Genetic causes of hearing loss;Willems;N Engl J Med,2000

3. Hereditary deafness and phenotyping in humans;Bitner-Glindzicz;Br Med Bull,2002

4. Non-syndromic, autosomal-recessive deafness;Petersen;Clin Genet,2006

5. Forty-six genes causing nonsyndromic hearing impairment: which ones should be analyzed in DNA diagnostics?;Hilgert;Mutat Res,2009

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1. A novel variant in GAS2 is associated with autosomal dominant nonsyndromic hearing impairment in a Chinese family;Human Genomics;2024-07-02

2. Unveiling a novel <italic>GJB2</italic> dominant K22T mutation in a Chinese family with hearing loss;Acta Biochimica et Biophysica Sinica;2024-05-01

3. Autosomal recessive non‐syndromic hearing loss genes in Pakistan during the previous three decades;Journal of Cellular and Molecular Medicine;2024-03-27

4. A novel Variant in GAS2 Is Associated with Non-Syndromic Autosomal Dominant Hearing Impairment in a Chinese Family;2024-02-14

5. Hearing Loss: Genetic Testing, Current Advances and the Situation in Latin America;Genes;2024-01-29

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