15161559

Source:http://linkedlifedata.com/resource/pubmed/id/15161559

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0017260, umls-concept:C0152035, umls-concept:C0936012, umls-concept:C2751659
pubmed:issue	5
pubmed:dateCreated	2004-5-26
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/7513795
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Glycerol Kinase
pubmed:status	MEDLINE
pubmed:month	May
pubmed:issn	0366-6999
pubmed:author	pubmed-author:ChenLi-yingLY, pubmed-author:JiangJunJ, pubmed-author:MaHong-weiHW, pubmed-author:MatsuoMasafumiM, pubmed-author:WangYue-pingYP, pubmed-author:WangZhi-chaoZC
pubmed:issnType	Print
pubmed:volume	117
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	789-91
pubmed:dateRevised	2005-11-17
pubmed:meshHeading	pubmed-meshheading:15161559-Adrenal Insufficiency, pubmed-meshheading:15161559-Child, Preschool, pubmed-meshheading:15161559-Chromosome Deletion, pubmed-meshheading:15161559-Chromosomes, Human, X, pubmed-meshheading:15161559-Gene Deletion, pubmed-meshheading:15161559-Glycerol Kinase, pubmed-meshheading:15161559-Humans, pubmed-meshheading:15161559-Male, pubmed-meshheading:15161559-Muscular Dystrophy, Duchenne, pubmed-meshheading:15161559-Sex Chromosome Aberrations
pubmed:year	2004
pubmed:articleTitle	Gene deletion analysis of a Chinese boy with Xp21 contiguous gene deletion syndrome.
pubmed:affiliation	Genetics Laboratory, Second Clinical College, China Medical University, Shenyang 110004, China. mahongwei1960@hotmail.com
pubmed:publicationType	Journal Article, Case Reports