10636744

Source:http://linkedlifedata.com/resource/pubmed/id/10636744

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0008654, umls-concept:C0030705, umls-concept:C0205210, umls-concept:C0449721, umls-concept:C1442161, umls-concept:C1521991, umls-concept:C2607943, umls-concept:C2926606
pubmed:issue	12
pubmed:dateCreated	2000-1-7
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/2985087R
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:month	Dec
pubmed:issn	0022-2593
pubmed:author	pubmed-author:BradyA FAF, pubmed-author:ElsawiM MMM, pubmed-author:JamiesonC RCR, pubmed-author:JefferySS, pubmed-author:MarksKK, pubmed-author:MurtazaLL, pubmed-author:PattonM AMA, pubmed-author:SavageM OMO
pubmed:issnType	Print
pubmed:volume	36
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	939-41
pubmed:dateRevised	2008-11-20
pubmed:meshHeading	pubmed-meshheading:10636744-Adolescent, pubmed-meshheading:10636744-Chromosome Deletion, pubmed-meshheading:10636744-Chromosomes, Human, Pair 12, pubmed-meshheading:10636744-Female, pubmed-meshheading:10636744-Humans, pubmed-meshheading:10636744-Microsatellite Repeats, pubmed-meshheading:10636744-Noonan Syndrome
pubmed:year	1999
pubmed:articleTitle	Clinical and molecular findings in a patient with a deletion on the long arm of chromosome 12.
pubmed:publicationType	Letter, Case Reports, Research Support, Non-U.S. Gov't