12362044

Source:http://linkedlifedata.com/resource/pubmed/id/12362044

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0015671, umls-concept:C0037683, umls-concept:C0205108, umls-concept:C0205182, umls-concept:C0205314, umls-concept:C0679622, umls-concept:C1442161, umls-concept:C1521104
pubmed:issue	10
pubmed:dateCreated	2002-10-3
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/2985087R
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:month	Oct
pubmed:issn	1468-6244
pubmed:author	pubmed-author:BurnsJ EJE, pubmed-author:FantesJJ, pubmed-author:Garcia-MiñaurSS, pubmed-author:MurrayR SRS, pubmed-author:PorteousM E MME, pubmed-author:StephenJJ, pubmed-author:StrainLL, pubmed-author:WarnerJ PJP
pubmed:issnType	Electronic
pubmed:volume	39
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	E62
pubmed:dateRevised	2008-11-20
pubmed:meshHeading	pubmed-meshheading:12362044-Adult, pubmed-meshheading:12362044-Chromosome Banding, pubmed-meshheading:12362044-Chromosome Deletion, pubmed-meshheading:12362044-Chromosomes, Human, Pair 22, pubmed-meshheading:12362044-Craniofacial Abnormalities, pubmed-meshheading:12362044-Humans, pubmed-meshheading:12362044-Infant, pubmed-meshheading:12362044-Karyotyping, pubmed-meshheading:12362044-Male, pubmed-meshheading:12362044-Nuclear Family, pubmed-meshheading:12362044-Syndrome, pubmed-meshheading:12362044-Tetralogy of Fallot
pubmed:year	2002
pubmed:articleTitle	A novel atypical 22q11.2 distal deletion in father and son.
pubmed:publicationType	Letter, Case Reports