10821562

Source:http://linkedlifedata.com/resource/pubmed/id/10821562

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0017380, umls-concept:C0439660, umls-concept:C0439825, umls-concept:C1384666
pubmed:issue	3
pubmed:dateCreated	2000-8-15
pubmed:abstractText	The application of molecular genetic techniques to the study of hereditary hearing impairment has contributed significantly to our understanding of auditory physiology and disease processes. This article reviews the current state of our knowledge regarding the genes associated with syndromic hereditary hearing impairment.
pubmed:grant	http://linkedlifedata.com/resource/pubmed/grant/KO8 DC00112
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/7909513
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:month	May
pubmed:issn	0192-9763
pubmed:author	pubmed-author:LalwaniA KAK, pubmed-author:TsengC JCJ
pubmed:issnType	Print
pubmed:volume	21
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	437-51
pubmed:dateRevised	2007-11-14
pubmed:meshHeading	pubmed-meshheading:10821562-Gene Expression, pubmed-meshheading:10821562-Genetic Code, pubmed-meshheading:10821562-Hearing, pubmed-meshheading:10821562-Hearing Disorders, pubmed-meshheading:10821562-Humans, pubmed-meshheading:10821562-Molecular Biology, pubmed-meshheading:10821562-Syndrome
pubmed:year	2000
pubmed:articleTitle	Cracking the auditory genetic code: part II. Syndromic hereditary hearing impairment.
pubmed:affiliation	Epstein Laboratories, Division of Otology, Neurotology, and Skull Base Surgery, University of California San Francisco, 94132-0342, USA.
pubmed:publicationType	Journal Article, Research Support, U.S. Gov't, P.H.S., Review, Research Support, Non-U.S. Gov't