20357662

Source:http://linkedlifedata.com/resource/pubmed/id/20357662

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0031437, umls-concept:C0205117, umls-concept:C1515448, umls-concept:C1524003, umls-concept:C2936346
pubmed:issue	3
pubmed:dateCreated	2010-6-9
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/9207893
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:month	Jul
pubmed:issn	1473-5717
pubmed:author	pubmed-author:MielooHannekeH, pubmed-author:OckeloenCharlotte WCW, pubmed-author:ReijnenIneke G MIG, pubmed-author:de LeeuwNicoleN, pubmed-author:de VriesBert B ABB
pubmed:issnType	Electronic
pubmed:volume	19
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	137-9
pubmed:meshHeading	pubmed-meshheading:20357662-Abnormalities, Multiple, pubmed-meshheading:20357662-Child, pubmed-meshheading:20357662-Child, Preschool, pubmed-meshheading:20357662-Chromosome Deletion, pubmed-meshheading:20357662-Chromosomes, Human, Pair 22, pubmed-meshheading:20357662-Chromosomes, Human, Pair 8, pubmed-meshheading:20357662-Female, pubmed-meshheading:20357662-Humans, pubmed-meshheading:20357662-Infant, pubmed-meshheading:20357662-Infant, Newborn, pubmed-meshheading:20357662-Phenotype, pubmed-meshheading:20357662-Pregnancy, pubmed-meshheading:20357662-Syndrome
pubmed:year	2010
pubmed:articleTitle	Two adjacent microdeletions in 8q11.2 cause a phenotype suggestive of the 22q11 deletion syndrome.
pubmed:affiliation	Department of Human Genetics, Radboud University, Nijmegen Medical Centre, Nijmegen, The Netherlands.
pubmed:publicationType	Journal Article, Case Reports, Research Support, Non-U.S. Gov't