9199579

Source:http://linkedlifedata.com/resource/pubmed/id/9199579

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0012236, umls-concept:C0205147, umls-concept:C0205182, umls-concept:C1442161, umls-concept:C1511545, umls-concept:C1511790, umls-concept:C1521101, umls-concept:C1948020
pubmed:issue	6
pubmed:dateCreated	1997-7-10
pubmed:commentsCorrections	http://linkedlifedata.com/resource/pubmed/commentcorrection/9199579-1349199, http://linkedlifedata.com/resource/pubmed/commentcorrection/9199579-1349369, http://linkedlifedata.com/resource/pubmed/commentcorrection/9199579-1355155, http://linkedlifedata.com/resource/pubmed/commentcorrection/9199579-1360769, http://linkedlifedata.com/resource/pubmed/commentcorrection/9199579-2045103, http://linkedlifedata.com/resource/pubmed/commentcorrection/9199579-7566101, http://linkedlifedata.com/resource/pubmed/commentcorrection/9199579-7633403, http://linkedlifedata.com/resource/pubmed/commentcorrection/9199579-7655455, http://linkedlifedata.com/resource/pubmed/commentcorrection/9199579-7670464, http://linkedlifedata.com/resource/pubmed/commentcorrection/9199579-7762561, http://linkedlifedata.com/resource/pubmed/commentcorrection/9199579-8111380, http://linkedlifedata.com/resource/pubmed/commentcorrection/9199579-8230157, http://linkedlifedata.com/resource/pubmed/commentcorrection/9199579-8651317, http://linkedlifedata.com/resource/pubmed/commentcorrection/9199579-8659529, http://linkedlifedata.com/resource/pubmed/commentcorrection/9199579-8776594, http://linkedlifedata.com/resource/pubmed/commentcorrection/9199579-8849001
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0370475
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Genetic Markers
pubmed:status	MEDLINE
pubmed:month	Jun
pubmed:issn	0002-9297
pubmed:author	pubmed-author:GouldCC, pubmed-author:McKeownCC, pubmed-author:MorrowBB, pubmed-author:O'DonnellHH, pubmed-author:ScamblerPP
pubmed:issnType	Print
pubmed:volume	60
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	1544-8
pubmed:dateRevised	2009-11-18
pubmed:meshHeading	pubmed-meshheading:9199579-Chromosome Deletion, pubmed-meshheading:9199579-Chromosome Mapping, pubmed-meshheading:9199579-Chromosomes, Human, Pair 22, pubmed-meshheading:9199579-DiGeorge Syndrome, pubmed-meshheading:9199579-Female, pubmed-meshheading:9199579-Genetic Markers, pubmed-meshheading:9199579-Humans, pubmed-meshheading:9199579-In Situ Hybridization, Fluorescence, pubmed-meshheading:9199579-Karyotyping, pubmed-meshheading:9199579-Male, pubmed-meshheading:9199579-Pedigree
pubmed:year	1997
pubmed:articleTitle	Detection of an atypical 22q11 deletion that has no overlap with the DiGeorge syndrome critical region.
pubmed:publicationType	Letter, Research Support, Non-U.S. Gov't