21143469

Source:http://linkedlifedata.com/resource/pubmed/id/21143469

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0015576, umls-concept:C0039082, umls-concept:C1422222, umls-concept:C1456348, umls-concept:C1551338, umls-concept:C2699782, umls-concept:C2827424
pubmed:issue	1
pubmed:dateCreated	2010-12-14
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0253664
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/WNT10A protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Wnt Proteins
pubmed:status	MEDLINE
pubmed:month	Jan
pubmed:issn	1399-0004
pubmed:author	pubmed-author:BrancatiFF, pubmed-author:CastigliaDD, pubmed-author:CastoroGG, pubmed-author:FischerJJ, pubmed-author:FloriddiaGG, pubmed-author:FoglioMM, pubmed-author:HeathSS, pubmed-author:MadonnaSS, pubmed-author:ZambrunoGG
pubmed:issnType	Electronic
pubmed:volume	79
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	92-5
pubmed:meshHeading	pubmed-meshheading:21143469-Aged, pubmed-meshheading:21143469-Amino Acid Sequence, pubmed-meshheading:21143469-Ectodermal Dysplasia, pubmed-meshheading:21143469-Exons, pubmed-meshheading:21143469-Female, pubmed-meshheading:21143469-Humans, pubmed-meshheading:21143469-Keratoderma, Palmoplantar, pubmed-meshheading:21143469-Male, pubmed-meshheading:21143469-Molecular Sequence Data, pubmed-meshheading:21143469-Mutation, pubmed-meshheading:21143469-Oligonucleotide Array Sequence Analysis, pubmed-meshheading:21143469-Pedigree, pubmed-meshheading:21143469-Wnt Proteins
pubmed:year	2011
pubmed:articleTitle	Two families confirm Schöpf-Schulz-Passarge syndrome as a discrete entity within the WNT10A phenotypic spectrum.
pubmed:publicationType	Letter, Research Support, Non-U.S. Gov't