20376788

Source:http://linkedlifedata.com/resource/pubmed/id/20376788

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0026882, umls-concept:C0030551, umls-concept:C0030705, umls-concept:C0035372, umls-concept:C0439659, umls-concept:C0936012, umls-concept:C1417098
pubmed:issue	2
pubmed:dateCreated	2010-4-8
pubmed:abstractText	To identify the parental origin of methyl-CpG-binding protein 2 (MECP2) gene mutations in Chinese patients with Rett syndrome.
pubmed:language	chi
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/9425197
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Methyl-CpG-Binding Protein 2
pubmed:status	MEDLINE
pubmed:month	Apr
pubmed:issn	1003-9406
pubmed:author	pubmed-author:BaoXin-huaXH, pubmed-author:CaoGuang-naGN, pubmed-author:JiaLi-fangLF, pubmed-author:JiangSheng-lingSL, pubmed-author:LuHong-meiHM, pubmed-author:PanHongH, pubmed-author:WuXi-ruXR, pubmed-author:ZhangJing-jingJJ, pubmed-author:ZhuXing-wangXW
pubmed:issnType	Print
pubmed:volume	27
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	121-4
pubmed:meshHeading	pubmed-meshheading:20376788-Base Sequence, pubmed-meshheading:20376788-Child, Preschool, pubmed-meshheading:20376788-DNA Mutational Analysis, pubmed-meshheading:20376788-Fathers, pubmed-meshheading:20376788-Female, pubmed-meshheading:20376788-Humans, pubmed-meshheading:20376788-Male, pubmed-meshheading:20376788-Methyl-CpG-Binding Protein 2, pubmed-meshheading:20376788-Mothers, pubmed-meshheading:20376788-Mutation, pubmed-meshheading:20376788-Parents, pubmed-meshheading:20376788-Polymorphism, Single Nucleotide, pubmed-meshheading:20376788-Rett Syndrome
pubmed:year	2010
pubmed:articleTitle	[Analysis of the parental origin of MECP2 mutations in patients with Rett syndrome].
pubmed:affiliation	Department of Pediatrics, Peking University First Hospital, Beijing, P.R. China.
pubmed:publicationType	Journal Article, English Abstract, Research Support, Non-U.S. Gov't