20503306

Source:http://linkedlifedata.com/resource/pubmed/id/20503306

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0015576, umls-concept:C0019904, umls-concept:C0020792, umls-concept:C1511760, umls-concept:C1824414, umls-concept:C1858723
pubmed:issue	6
pubmed:dateCreated	2010-5-26
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/101235741
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:month	Jun
pubmed:issn	1552-4833
pubmed:author	pubmed-author:HideMichihiroM, pubmed-author:LacombeDidierD, pubmed-author:McGrathJohnJ, pubmed-author:Morice-PicardFannyF, pubmed-author:NagyNikolettaN, pubmed-author:TaïebAlainA, pubmed-author:TanakaAkioA
pubmed:issnType	Electronic
pubmed:volume	152A
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	1347-8
pubmed:dateRevised	2010-11-18
pubmed:meshHeading	pubmed-meshheading:20503306-Chromosomes, Human, Pair 16, pubmed-meshheading:20503306-DNA Mutational Analysis, pubmed-meshheading:20503306-Gene Deletion, pubmed-meshheading:20503306-Genetic Linkage, pubmed-meshheading:20503306-Humans, pubmed-meshheading:20503306-Lod Score, pubmed-meshheading:20503306-Neutropenia, pubmed-meshheading:20503306-Open Reading Frames, pubmed-meshheading:20503306-Pedigree, pubmed-meshheading:20503306-Polymorphism, Single Nucleotide, pubmed-meshheading:20503306-Rothmund-Thomson Syndrome
pubmed:year	2010
pubmed:articleTitle	Identification of a homozygous deletion mutation in C16orf57 in a family with Clericuzio-type poikiloderma with neutropenia.
pubmed:affiliation	St John's Institute of Dermatology, King's College London (Guy's Campus), London, UK.
pubmed:publicationType	Journal Article