8702120

Source:http://linkedlifedata.com/resource/pubmed/id/8702120

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0017337, umls-concept:C0026882, umls-concept:C0031437, umls-concept:C0205171, umls-concept:C0678226, umls-concept:C1522384, umls-concept:C1861922, umls-concept:C1880371
pubmed:dateCreated	1996-9-3
pubmed:grant	http://linkedlifedata.com/resource/pubmed/grant/
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/7506858
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/High Mobility Group Proteins, http://linkedlifedata.com/resource/pubmed/chemical/SOX9 Transcription Factor, http://linkedlifedata.com/resource/pubmed/chemical/SOX9 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Transcription Factors
pubmed:status	MEDLINE
pubmed:month	Jun
pubmed:issn	0077-8923
pubmed:author	pubmed-author:FosterJ WJW, pubmed-author:GoodfellowP NPN, pubmed-author:GuioliSS, pubmed-author:KwokCC, pubmed-author:SchaferA JAJ, pubmed-author:WellerP APA
pubmed:issnType	Print
pubmed:day	8
pubmed:volume	785
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	137-49
pubmed:dateRevised	2010-11-18
pubmed:meshHeading	pubmed-meshheading:8702120-Abnormalities, Multiple, pubmed-meshheading:8702120-Bone and Bones, pubmed-meshheading:8702120-Chromosomes, Human, Pair 17, pubmed-meshheading:8702120-Chromosomes, Human, Pair 2, pubmed-meshheading:8702120-Disorders of Sex Development, pubmed-meshheading:8702120-Female, pubmed-meshheading:8702120-High Mobility Group Proteins, pubmed-meshheading:8702120-Humans, pubmed-meshheading:8702120-Male, pubmed-meshheading:8702120-Mutation, pubmed-meshheading:8702120-Osteochondrodysplasias, pubmed-meshheading:8702120-Phenotype, pubmed-meshheading:8702120-SOX9 Transcription Factor, pubmed-meshheading:8702120-Sex Differentiation, pubmed-meshheading:8702120-Transcription Factors, pubmed-meshheading:8702120-Translocation, Genetic, pubmed-meshheading:8702120-X Chromosome, pubmed-meshheading:8702120-Y Chromosome
pubmed:year	1996
pubmed:articleTitle	Campomelic dysplasia with XY sex reversal: diverse phenotypes resulting from mutations in a single gene.
pubmed:affiliation	Department of Genetics, University of Cambridge, UK.
pubmed:publicationType	Journal Article, Review, Research Support, Non-U.S. Gov't