Non-syndromic dominant sensorineural hearing loss: from a few phenotypes to many genotypes-Reference-Cited by-同舟云学术

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Non-syndromic dominant sensorineural hearing loss: from a few phenotypes to many genotypes

Published:1997-01 Issue:3 Volume:38 Page:237-245
ISSN:0165-5876
Container-title:International Journal of Pediatric Otorhinolaryngology
language:en
Short-container-title:International Journal of Pediatric Otorhinolaryngology

Author:

Stinckens Christel,Ensink Robbert,Feenstra Louw,Fryns Jean-Pierre,Cremers Cor

Publisher

Elsevier BV

Subject

Otorhinolaryngology,General Medicine,Pediatrics, Perinatology, and Child Health

Reference47 articles.

1. Hereditary hearing loss and its syndromes;Gorlin,1995

2. Genetics of hearing impairment;Brunner;Ann. N.Y. Acad. Sci.,1991

3. Mitochondrial genetics and deafness;Reardon;J. Audiol. Med.,1995

4. Non-Mendelian mitochondrial inheritance as a cause of progressive sensorineural hearing loss;Gold;Int. J. Ped. ORL.,1994

5. Gene linkage and genetic deafness;Cremers;Int. J. Ped. ORL.,1995

Cited by 1 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. Non-Syndromal Autosomal Dominant Hearing Impairment: Ongoing Phenotypical Characterization of Genotypes;British Journal of Audiology;1999-01

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