12923874

Source:http://linkedlifedata.com/resource/pubmed/id/12923874

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0007570, umls-concept:C0030705, umls-concept:C0220704, umls-concept:C0220908, umls-concept:C2910370
pubmed:issue	3
pubmed:dateCreated	2003-8-18
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/101235741
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:month	Sep
pubmed:issn	1552-4825
pubmed:author	pubmed-author:CastroMassimoM, pubmed-author:ColistroFrancoF, pubmed-author:DallapiccolaBrunoB, pubmed-author:DigilioMaria CristinaMC, pubmed-author:FerrettiFrancescaF, pubmed-author:GiannottiAldoA, pubmed-author:MarinoBrunoB
pubmed:issnType	Print
pubmed:day	1
pubmed:volume	121A
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	286-8
pubmed:dateRevised	2008-5-21
pubmed:meshHeading	pubmed-meshheading:12923874-Abnormalities, Multiple, pubmed-meshheading:12923874-Adolescent, pubmed-meshheading:12923874-Celiac Disease, pubmed-meshheading:12923874-Child, pubmed-meshheading:12923874-Child, Preschool, pubmed-meshheading:12923874-Chromosome Deletion, pubmed-meshheading:12923874-Chromosomes, Human, Pair 22, pubmed-meshheading:12923874-DiGeorge Syndrome, pubmed-meshheading:12923874-Face, pubmed-meshheading:12923874-Female, pubmed-meshheading:12923874-Humans, pubmed-meshheading:12923874-Male, pubmed-meshheading:12923874-Phenotype, pubmed-meshheading:12923874-Velopharyngeal Insufficiency
pubmed:year	2003
pubmed:articleTitle	Screening for celiac disease in patients with deletion 22q11.2 (DiGeorge/velo-cardio-facial syndrome).
pubmed:publicationType	Letter