20095987

Source:http://linkedlifedata.com/resource/pubmed/id/20095987

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0205210, umls-concept:C0265205, umls-concept:C1442161, umls-concept:C2348519
pubmed:issue	4
pubmed:dateCreated	2010-5-7
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0253664
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:month	Apr
pubmed:issn	1399-0004
pubmed:author	pubmed-author:BrunnerH GHG, pubmed-author:KrepischiA C VAC, pubmed-author:MaccraughanJJ, pubmed-author:MazzeuJ FJF, pubmed-author:McGillJJ, pubmed-author:OudakkerAA, pubmed-author:RosenbergCC, pubmed-author:SzuhaiKK, pubmed-author:Vianna-MorganteA MAM, pubmed-author:van BokhovenHH
pubmed:issnType	Electronic
pubmed:volume	77
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	404-7
pubmed:meshHeading	pubmed-meshheading:20095987-Abnormalities, Multiple, pubmed-meshheading:20095987-Child, pubmed-meshheading:20095987-Child, Preschool, pubmed-meshheading:20095987-Chromosome Breakage, pubmed-meshheading:20095987-Chromosome Deletion, pubmed-meshheading:20095987-Chromosomes, Human, Pair 1, pubmed-meshheading:20095987-Female, pubmed-meshheading:20095987-Genes, Dominant, pubmed-meshheading:20095987-Humans, pubmed-meshheading:20095987-Infant, pubmed-meshheading:20095987-Male, pubmed-meshheading:20095987-Syndrome
pubmed:year	2010
pubmed:articleTitle	Deletions encompassing 1q41q42.1 and clinical features of autosomal dominant Robinow syndrome.
pubmed:affiliation	Departamento de Genética e Biologia Evolutiva, Instituto de Biociências, Universidade de São Paulo, Brazil.
pubmed:publicationType	Journal Article, Case Reports