20137643

Source:http://linkedlifedata.com/resource/pubmed/id/20137643

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0004083, umls-concept:C0012655, umls-concept:C0032659, umls-concept:C0152035, umls-concept:C0559260, umls-concept:C0678951, umls-concept:C1420068, umls-concept:C1551910, umls-concept:C2603343
pubmed:issue	41
pubmed:dateCreated	2010-2-8
pubmed:abstractText	To investigate whether polymorphisms of SIM2 gene are associated with congenital scoliosis (CS) in a Chinese Han population. and explore the relationship of between polymorphisms of SIM2 and clinical phenotypes of CS.
pubmed:language	chi
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/7511141
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Basic Helix-Loop-Helix..., http://linkedlifedata.com/resource/pubmed/chemical/SIM2 protein, human
pubmed:status	MEDLINE
pubmed:month	Nov
pubmed:issn	0376-2491
pubmed:author	pubmed-author:QiuGui-xingGX, pubmed-author:WangHaiH, pubmed-author:WangNai-guoNG, pubmed-author:WangYi-pengYP, pubmed-author:WuZhi-hongZH, pubmed-author:YinRuo-fengRF, pubmed-author:YuH FHF, pubmed-author:ZhouXiX
pubmed:issnType	Print
pubmed:day	10
pubmed:volume	89
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	2888-93
pubmed:meshHeading	pubmed-meshheading:20137643-Adolescent, pubmed-meshheading:20137643-Alleles, pubmed-meshheading:20137643-Asian Continental Ancestry Group, pubmed-meshheading:20137643-Basic Helix-Loop-Helix Transcription Factors, pubmed-meshheading:20137643-Case-Control Studies, pubmed-meshheading:20137643-Child, pubmed-meshheading:20137643-Child, Preschool, pubmed-meshheading:20137643-Chromosome Mapping, pubmed-meshheading:20137643-Female, pubmed-meshheading:20137643-Genetic Predisposition to Disease, pubmed-meshheading:20137643-Genome-Wide Association Study, pubmed-meshheading:20137643-Genotype, pubmed-meshheading:20137643-Humans, pubmed-meshheading:20137643-Male, pubmed-meshheading:20137643-Phenotype, pubmed-meshheading:20137643-Polymorphism, Single Nucleotide, pubmed-meshheading:20137643-Scoliosis, pubmed-meshheading:20137643-Young Adult
pubmed:year	2009
pubmed:articleTitle	[Association study of SIM2 gene polymorphisms with susceptibility to congenital scoliosis in a Chinese Han population].
pubmed:affiliation	Department of Orthopedics, Beijing Friendship Hospital, Capital Medical University, Beijing 100050, China.
pubmed:publicationType	Journal Article, English Abstract