Art
J-GLOBAL ID：201102272791660904   Reference number：11A0838139

Molecular diagnosis of deafness

難聴の遺伝子診断
Author (1)：
USAMI SHIN'ICHI

About USAMI SHIN'ICHI

(信州大学医学部耳鼻咽喉科学講座)

About 信州大学医学部耳鼻咽喉科学講座


Material：
Audiology Japan  (Audiol Jpn)

About Audiology Japan


Volume： 54  Issue： 1  Page： 44-55 (J-STAGE)  Publication year： 2011 
JST Material Number： Z0102B  ISSN： 0303-8106  Document type： Article
Article type： 文献レビュー  Country of issue： Japan (JPN)  Language： JAPANESE (JA)
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gene diagnosis

About gene diagnosis

,...
Semi thesaurus term：
Thesaurus term/Semi thesaurus term
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All keywords is available on JDreamIII(charged).
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*Congenital deafness

About Congenital deafness


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JST classification (2)：
JST classification
Category name(code) classified by JST.
Otorhinolaryngologic diagnosis 
(GQ02000Q)

About Otorhinolaryngologic diagnosis

,  Diagnostics of congenital diseases, deformities. 
(GD03020G)

About Diagnostics of congenital diseases, deformities.

Reference (30)：
  • MORTON, CC. Newborn hearing screening-A silent revolution. N Engl J Med. 2006, 354, 2151-2164
  • VAN CAMP, G. Hereditary Hearing Loss Homepage. http://hereditaryhearingloss.org
  • 宇佐美真一. 日本人難聴遺伝子データベースホームページ. http://ent.md.shinshu-u.ac.jp/deafgene.html
  • USAMI, S. The responsible genes in Japanese deafness patients and clinical application using Invader assay. Acta Otolaryngol. 2008, 128, 446-454
  • OHTSUKA, A. GJB2 deafness gene shows a specific spectrum of mutations in Japan, including a frequent founder mutation. Hum Genet. 2003, 112, 329-333
ｍore...
Terms in the title (2)：
Terms in the title
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難聴

About 難聴

, 
遺伝子診断

About 遺伝子診断


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