11186941

Source:http://linkedlifedata.com/resource/pubmed/id/11186941

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0019904, umls-concept:C0024554, umls-concept:C0079822, umls-concept:C0432230, umls-concept:C1420041, umls-concept:C1442161
pubmed:issue	12
pubmed:dateCreated	2000-12-12
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/2985087R
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Homeodomain Proteins, http://linkedlifedata.com/resource/pubmed/chemical/SHOX protein, human
pubmed:status	MEDLINE
pubmed:month	Dec
pubmed:issn	1468-6244
pubmed:author	pubmed-author:AftimosSS, pubmed-author:OedMM, pubmed-author:RobertsonS PSP, pubmed-author:SavarirayanRR, pubmed-author:ScamblerP JPJ, pubmed-author:ShearsD JDJ, pubmed-author:WinterR MRM
pubmed:issnType	Electronic
pubmed:volume	37
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	959-64
pubmed:dateRevised	2011-11-17
pubmed:meshHeading	pubmed-meshheading:11186941-Adolescent, pubmed-meshheading:11186941-Child, pubmed-meshheading:11186941-Child, Preschool, pubmed-meshheading:11186941-Female, pubmed-meshheading:11186941-Gene Deletion, pubmed-meshheading:11186941-Genes, Homeobox, pubmed-meshheading:11186941-Homeodomain Proteins, pubmed-meshheading:11186941-Homozygote, pubmed-meshheading:11186941-Humans, pubmed-meshheading:11186941-Intellectual Disability, pubmed-meshheading:11186941-Male, pubmed-meshheading:11186941-Osteochondrodysplasias, pubmed-meshheading:11186941-Pedigree
pubmed:year	2000
pubmed:articleTitle	Homozygous deletion of SHOX in a mentally retarded male with Langer mesomelic dysplasia.
pubmed:publicationType	Letter, Case Reports, Research Support, Non-U.S. Gov't