11594342

Source:http://linkedlifedata.com/resource/pubmed/id/11594342

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0017337, umls-concept:C0024554, umls-concept:C0036341, umls-concept:C0086418, umls-concept:C0205147, umls-concept:C0205369, umls-concept:C1334043, umls-concept:C1366449, umls-concept:C1538631, umls-concept:C1539607, umls-concept:C1825005, umls-concept:C2697616
pubmed:issue	10
pubmed:dateCreated	2001-10-10
pubmed:databankReference	http://linkedlifedata.com/resource/pubmed/xref/GENBANK/AJ309278
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:AffaraN ANA, pubmed-author:BoucherC ACA, pubmed-author:CrowT JTJ, pubmed-author:NankoSS, pubmed-author:RossN LNL, pubmed-author:SargentC ACA, pubmed-author:WadekarRR, pubmed-author:WilliamsN ANA, pubmed-author:YangJJ
pubmed:issnType	Electronic
pubmed:volume	38
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	710-9
pubmed:dateRevised	2008-11-20
pubmed:meshHeading	pubmed-meshheading:11594342-Asian Continental Ancestry Group, pubmed-meshheading:11594342-Base Sequence, pubmed-meshheading:11594342-Cell Line, Transformed, pubmed-meshheading:11594342-Chromosome Breakage, pubmed-meshheading:11594342-Cloning, Molecular, pubmed-meshheading:11594342-Gene Amplification, pubmed-meshheading:11594342-Genes, Duplicate, pubmed-meshheading:11594342-Humans, pubmed-meshheading:11594342-In Situ Hybridization, Fluorescence, pubmed-meshheading:11594342-Japan, pubmed-meshheading:11594342-Male, pubmed-meshheading:11594342-Microsatellite Repeats, pubmed-meshheading:11594342-Molecular Sequence Data, pubmed-meshheading:11594342-Polymerase Chain Reaction, pubmed-meshheading:11594342-Radiation Hybrid Mapping, pubmed-meshheading:11594342-Restriction Mapping, pubmed-meshheading:11594342-Schizophrenia, pubmed-meshheading:11594342-Sequence Homology, Nucleic Acid, pubmed-meshheading:11594342-Sequence Tagged Sites, pubmed-meshheading:11594342-Sex Chromosome Disorders, pubmed-meshheading:11594342-Translocation, Genetic, pubmed-meshheading:11594342-X Chromosome, pubmed-meshheading:11594342-Y Chromosome
pubmed:year	2001
pubmed:articleTitle	Triplication of several PAR1 genes and part of the Homo sapiens specific Yp11.2/Xq21.3 region of homology in a 46,X,t(X;Y)(p22.33;p11.2) male with schizophrenia.
pubmed:publicationType	Letter, Case Reports, Research Support, Non-U.S. Gov't