12131871

Source:http://linkedlifedata.com/resource/pubmed/id/12131871

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0012236, umls-concept:C0220704, umls-concept:C0332162, umls-concept:C1280464, umls-concept:C2676337
pubmed:issue	4
pubmed:dateCreated	2002-7-19
pubmed:language	ita
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0400740
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:month	Aug
pubmed:issn	0026-4946
pubmed:author	pubmed-author:BertoneAA, pubmed-author:CampraDD, pubmed-author:GualaAA, pubmed-author:PontorieroDD, pubmed-author:PuscedduMM
pubmed:issnType	Print
pubmed:volume	54
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	343-5
pubmed:dateRevised	2006-3-28
pubmed:meshHeading	pubmed-meshheading:12131871-Chromosome Deletion, pubmed-meshheading:12131871-Chromosomes, Human, Pair 22, pubmed-meshheading:12131871-Craniofacial Abnormalities, pubmed-meshheading:12131871-DiGeorge Syndrome, pubmed-meshheading:12131871-Diagnosis, Differential, pubmed-meshheading:12131871-Heart Defects, Congenital, pubmed-meshheading:12131871-Humans, pubmed-meshheading:12131871-Hypocalcemia, pubmed-meshheading:12131871-Hypoparathyroidism, pubmed-meshheading:12131871-Infant, pubmed-meshheading:12131871-Infant, Newborn, pubmed-meshheading:12131871-Male
pubmed:year	2002
pubmed:articleTitle	[Transient neonatal hypocalcemia. Onset Manifestation of the 22q11.2 deletion syndrome].
pubmed:publicationType	Letter, Case Reports