11183182

Source:http://linkedlifedata.com/resource/pubmed/id/11183182

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0265264, umls-concept:C1513780
pubmed:issue	10
pubmed:dateCreated	2000-10-12
pubmed:databankReference	http://linkedlifedata.com/resource/pubmed/xref/GENBANK/AF221714
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:Armstrong-BuisseretLL, pubmed-author:BonnetDD, pubmed-author:ChingY HYH, pubmed-author:CrossS JSJ, pubmed-author:GardinerC ACA, pubmed-author:JonveauxPP, pubmed-author:LeheupBB, pubmed-author:LiQ YQY, pubmed-author:LyonnetSS, pubmed-author:MortierGG, pubmed-author:PenttinenMM, pubmed-author:SprangerSS, pubmed-author:Van RavenswaaijCC
pubmed:issnType	Electronic
pubmed:volume	37
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	785-7
pubmed:dateRevised	2009-11-19
pubmed:meshHeading	pubmed-meshheading:11183182-Chromosome Mapping, pubmed-meshheading:11183182-Chromosomes, Human, Pair 12, pubmed-meshheading:11183182-DNA Mutational Analysis, pubmed-meshheading:11183182-Exons, pubmed-meshheading:11183182-Female, pubmed-meshheading:11183182-Genetic Testing, pubmed-meshheading:11183182-Genetic Variation, pubmed-meshheading:11183182-Genotype, pubmed-meshheading:11183182-Heart Block, pubmed-meshheading:11183182-Heart Defects, Congenital, pubmed-meshheading:11183182-Heart Septal Defects, pubmed-meshheading:11183182-Humans, pubmed-meshheading:11183182-Introns, pubmed-meshheading:11183182-Limb Deformities, Congenital, pubmed-meshheading:11183182-Male, pubmed-meshheading:11183182-Molecular Sequence Data, pubmed-meshheading:11183182-Mutation, pubmed-meshheading:11183182-Pedigree, pubmed-meshheading:11183182-Phenotype, pubmed-meshheading:11183182-Polymorphism, Single-Stranded Conformational, pubmed-meshheading:11183182-Syndactyly, pubmed-meshheading:11183182-Syndrome
pubmed:year	2000
pubmed:articleTitle	The mutation spectrum in Holt-Oram syndrome.
pubmed:publicationType	Letter