16199542

Source:http://linkedlifedata.com/resource/pubmed/id/16199542

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0007194, umls-concept:C0010210, umls-concept:C0026882, umls-concept:C0030705, umls-concept:C0205173, umls-concept:C0205198, umls-concept:C0679560
pubmed:issue	10
pubmed:dateCreated	2005-10-3
pubmed:abstractText	To report the frequency of single and multiple gene mutations in an Australian cohort of patients with hypertrophic cardiomyopathy (HCM).
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:ChiuCC, pubmed-author:DoolanAA, pubmed-author:InglesJJ, pubmed-author:SeidmanCC, pubmed-author:SeidmanJJ, pubmed-author:SemsarianCC
pubmed:issnType	Electronic
pubmed:volume	42
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	e59
pubmed:dateRevised	2008-11-20
pubmed:meshHeading	pubmed-meshheading:16199542-Adolescent, pubmed-meshheading:16199542-Adult, pubmed-meshheading:16199542-Aged, pubmed-meshheading:16199542-Aged, 80 and over, pubmed-meshheading:16199542-Cardiomyopathy, Hypertrophic, pubmed-meshheading:16199542-Chromatography, High Pressure Liquid, pubmed-meshheading:16199542-Cohort Studies, pubmed-meshheading:16199542-Female, pubmed-meshheading:16199542-Genetic Counseling, pubmed-meshheading:16199542-Genetic Predisposition to Disease, pubmed-meshheading:16199542-Humans, pubmed-meshheading:16199542-Male, pubmed-meshheading:16199542-Middle Aged, pubmed-meshheading:16199542-Molecular Diagnostic Techniques, pubmed-meshheading:16199542-Mutation, pubmed-meshheading:16199542-Pedigree, pubmed-meshheading:16199542-Phenotype, pubmed-meshheading:16199542-Sequence Analysis, DNA
pubmed:year	2005
pubmed:articleTitle	Compound and double mutations in patients with hypertrophic cardiomyopathy: implications for genetic testing and counselling.
pubmed:publicationType	Letter, Research Support, Non-U.S. Gov't