20664692

Source:http://linkedlifedata.com/resource/pubmed/id/20664692

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0026882, umls-concept:C0030705, umls-concept:C0152035, umls-concept:C0683325, umls-concept:C1335192, umls-concept:C1847800
pubmed:dateCreated	2010-7-28
pubmed:abstractText	To detect paired box gene 3 (PAX3) mutations and associated phenotypes in Chinese patients with Waardenburg syndrome type 1 (WS1).
pubmed:commentsCorrections	http://linkedlifedata.com/resource/pubmed/commentcorrection/20664692-11057219, http://linkedlifedata.com/resource/pubmed/commentcorrection/20664692-11231058, http://linkedlifedata.com/resource/pubmed/commentcorrection/20664692-11810298, http://linkedlifedata.com/resource/pubmed/commentcorrection/20664692-12408085, http://linkedlifedata.com/resource/pubmed/commentcorrection/20664692-12444107, http://linkedlifedata.com/resource/pubmed/commentcorrection/20664692-12666593, http://linkedlifedata.com/resource/pubmed/commentcorrection/20664692-1349198, http://linkedlifedata.com/resource/pubmed/commentcorrection/20664692-14902764, http://linkedlifedata.com/resource/pubmed/commentcorrection/20664692-15148315, http://linkedlifedata.com/resource/pubmed/commentcorrection/20664692-1576755, http://linkedlifedata.com/resource/pubmed/commentcorrection/20664692-1682057, http://linkedlifedata.com/resource/pubmed/commentcorrection/20664692-16971891, http://linkedlifedata.com/resource/pubmed/commentcorrection/20664692-17254487, http://linkedlifedata.com/resource/pubmed/commentcorrection/20664692-17277738, http://linkedlifedata.com/resource/pubmed/commentcorrection/20664692-17323927, http://linkedlifedata.com/resource/pubmed/commentcorrection/20664692-17999358, http://linkedlifedata.com/resource/pubmed/commentcorrection/20664692-18761541, http://linkedlifedata.com/resource/pubmed/commentcorrection/20664692-20127975, http://linkedlifedata.com/resource/pubmed/commentcorrection/20664692-331943, http://linkedlifedata.com/resource/pubmed/commentcorrection/20664692-7874167, http://linkedlifedata.com/resource/pubmed/commentcorrection/20664692-7942851, http://linkedlifedata.com/resource/pubmed/commentcorrection/20664692-7981674, http://linkedlifedata.com/resource/pubmed/commentcorrection/20664692-8001158, http://linkedlifedata.com/resource/pubmed/commentcorrection/20664692-8019556, http://linkedlifedata.com/resource/pubmed/commentcorrection/20664692-8103404, http://linkedlifedata.com/resource/pubmed/commentcorrection/20664692-8490648, http://linkedlifedata.com/resource/pubmed/commentcorrection/20664692-8630502, http://linkedlifedata.com/resource/pubmed/commentcorrection/20664692-9170158, http://linkedlifedata.com/resource/pubmed/commentcorrection/20664692-9279758, http://linkedlifedata.com/resource/pubmed/commentcorrection/20664692-9462749
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/9605351
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/PAX3 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Paired Box Transcription Factors
pubmed:status	MEDLINE
pubmed:issn	1090-0535
pubmed:author	pubmed-author:GuoXiangmingX, pubmed-author:LiShiqiangS, pubmed-author:WangJuanJ, pubmed-author:WangPanfengP, pubmed-author:XiaoXueshanX, pubmed-author:ZhangQingjiongQ
pubmed:issnType	Electronic
pubmed:volume	16
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	1146-53
pubmed:meshHeading	pubmed-meshheading:20664692-Asian Continental Ancestry Group, pubmed-meshheading:20664692-Base Sequence, pubmed-meshheading:20664692-Case-Control Studies, pubmed-meshheading:20664692-China, pubmed-meshheading:20664692-DNA Mutational Analysis, pubmed-meshheading:20664692-Family, pubmed-meshheading:20664692-Female, pubmed-meshheading:20664692-Fundus Oculi, pubmed-meshheading:20664692-Humans, pubmed-meshheading:20664692-Male, pubmed-meshheading:20664692-Molecular Sequence Data, pubmed-meshheading:20664692-Mutation, pubmed-meshheading:20664692-Paired Box Transcription Factors, pubmed-meshheading:20664692-Pedigree, pubmed-meshheading:20664692-Phenotype, pubmed-meshheading:20664692-Waardenburg's Syndrome
pubmed:year	2010
pubmed:articleTitle	PAX3 mutations and clinical characteristics in Chinese patients with Waardenburg syndrome type 1.
pubmed:affiliation	State Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-sen University, Guangzhou, PR China.
pubmed:publicationType	Journal Article, Research Support, Non-U.S. Gov't