21271649

Source:http://linkedlifedata.com/resource/pubmed/id/21271649

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0015385, umls-concept:C0026882, umls-concept:C0030797, umls-concept:C0039082, umls-concept:C0243065, umls-concept:C0314603, umls-concept:C1337005, umls-concept:C1881065
pubmed:issue	2
pubmed:dateCreated	2011-1-28
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/101235741
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/WNT7A protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Wnt Proteins
pubmed:status	MEDLINE
pubmed:month	Feb
pubmed:issn	1552-4833
pubmed:author	pubmed-author:FerrariAdrianoA, pubmed-author:GaravelliLiviaL, pubmed-author:GelminiChiaraC, pubmed-author:LauschEkkehartE, pubmed-author:MariFrancescaF, pubmed-author:ReverberiSandroS, pubmed-author:RosatoSimonettaS, pubmed-author:SassiSilviaS, pubmed-author:Superti-FurgaAndreaA, pubmed-author:UngerSheilaS, pubmed-author:WischmeijerAnitaA, pubmed-author:ZabelBernhardB
pubmed:issnType	Electronic
pubmed:volume	155A
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	332-6
pubmed:dateRevised	2011-6-7
pubmed:meshHeading	pubmed-meshheading:21271649-Abnormalities, Multiple, pubmed-meshheading:21271649-Amino Acid Sequence, pubmed-meshheading:21271649-Base Sequence, pubmed-meshheading:21271649-Diagnosis, Differential, pubmed-meshheading:21271649-Female, pubmed-meshheading:21271649-Foot Deformities, Congenital, pubmed-meshheading:21271649-Hand Deformities, Congenital, pubmed-meshheading:21271649-Humans, pubmed-meshheading:21271649-Infant, pubmed-meshheading:21271649-Limb Deformities, Congenital, pubmed-meshheading:21271649-Male, pubmed-meshheading:21271649-Molecular Sequence Data, pubmed-meshheading:21271649-Mutation, Missense, pubmed-meshheading:21271649-Pelvis, pubmed-meshheading:21271649-Phenotype, pubmed-meshheading:21271649-Sequence Analysis, DNA, pubmed-meshheading:21271649-Syndrome, pubmed-meshheading:21271649-Uterus, pubmed-meshheading:21271649-Wnt Proteins
pubmed:year	2011
pubmed:articleTitle	Al-Awadi-Raas-Rothschild (limb/pelvis/uterus-hypoplasia/aplasia) syndrome and WNT7A mutations: genetic homogeneity and nosological delineation.
pubmed:affiliation	Clinical Genetics Unit, Obstetric and Pediatric Department, S. Maria Nuova Hospital, Reggio Emilia, Italy.
pubmed:publicationType	Journal Article, Comparative Study, Case Reports, Research Support, Non-U.S. Gov't