16454982

Source:http://linkedlifedata.com/resource/pubmed/id/16454982

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0030705, umls-concept:C0152035, umls-concept:C0205314, umls-concept:C0265237, umls-concept:C0596611, umls-concept:C0679622, umls-concept:C1412815
pubmed:issue	1
pubmed:dateCreated	2006-2-3
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/7513795
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/FOXL2 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Forkhead Transcription Factors
pubmed:status	MEDLINE
pubmed:month	Jan
pubmed:issn	0366-6999
pubmed:author	pubmed-author:LamTak-sum StephenTS, pubmed-author:LoFai-man IvanFM, pubmed-author:OrSiu-fong JuneSF, pubmed-author:TongMing-for TonyMF
pubmed:issnType	Print
pubmed:day	5
pubmed:volume	119
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	49-52
pubmed:meshHeading	pubmed-meshheading:16454982-Abnormalities, Multiple, pubmed-meshheading:16454982-Amino Acid Sequence, pubmed-meshheading:16454982-Blepharophimosis, pubmed-meshheading:16454982-Blepharoptosis, pubmed-meshheading:16454982-Eyelids, pubmed-meshheading:16454982-Female, pubmed-meshheading:16454982-Forkhead Transcription Factors, pubmed-meshheading:16454982-Humans, pubmed-meshheading:16454982-Male, pubmed-meshheading:16454982-Molecular Sequence Data, pubmed-meshheading:16454982-Mutation, pubmed-meshheading:16454982-Syndrome
pubmed:year	2006
pubmed:articleTitle	Three novel FOXL2 gene mutations in Chinese patients with blepharophimosis-ptosis-epicanthus inversus syndrome.
pubmed:affiliation	Clinical Genetic Service, Department of Health, Hong Kong SAR, China.
pubmed:publicationType	Journal Article