11836364

Source:http://linkedlifedata.com/resource/pubmed/id/11836364

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0026882, umls-concept:C0205314, umls-concept:C0205419, umls-concept:C0268363, umls-concept:C0679622, umls-concept:C0972255, umls-concept:C1314792, umls-concept:C1332773
pubmed:issue	2
pubmed:dateCreated	2002-2-11
pubmed:grant	http://linkedlifedata.com/resource/pubmed/grant/AR41223
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/2985087R
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:month	Feb
pubmed:issn	1468-6244
pubmed:author	pubmed-author:ByersP HPH, pubmed-author:HeegerSS, pubmed-author:JohnsonM TMT, pubmed-author:MooneySS, pubmed-author:MorrisonSS, pubmed-author:RobinN HNH
pubmed:issnType	Electronic
pubmed:volume	39
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	128-32
pubmed:dateRevised	2008-11-20
pubmed:meshHeading	pubmed-meshheading:11836364-Adult, pubmed-meshheading:11836364-Bone Diseases, Developmental, pubmed-meshheading:11836364-Female, pubmed-meshheading:11836364-Femur, pubmed-meshheading:11836364-Humans, pubmed-meshheading:11836364-Osteogenesis Imperfecta, pubmed-meshheading:11836364-Pregnancy, pubmed-meshheading:11836364-Prenatal Diagnosis
pubmed:year	2002
pubmed:articleTitle	A variant of osteogenesis imperfecta type IV with resolving kyphomelia is caused by a novel COL1A2 mutation.
pubmed:publicationType	Letter, Research Support, U.S. Gov't, P.H.S., Case Reports