15824798

Source:http://linkedlifedata.com/resource/pubmed/id/15824798

Download in:

Switch to

Custom View

Named Graph Language Inference

Statements in which the resource exists as a subject.
Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0017382, umls-concept:C0027126, umls-concept:C0030705, umls-concept:C0086543, umls-concept:C0220908, umls-concept:C0332307, umls-concept:C1513388
pubmed:issue	1
pubmed:dateCreated	2005-4-12
pubmed:abstractText	To detect MD1 premutation and full mutation carriers among cataract patients and offer familial genetic counseling.
pubmed:language	por
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0400645
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:issn	0004-2749
pubmed:author	pubmed-author:ChimelliLeila Maria CardãoLM, pubmed-author:RojasMaría Verónica MuñozMV, pubmed-author:SimõesAguinaldo LuizAL
pubmed:issnType	Print
pubmed:volume	68
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	15-20
pubmed:dateRevised	2009-11-19
pubmed:meshHeading	pubmed-meshheading:15824798-Adult, pubmed-meshheading:15824798-Cataract, pubmed-meshheading:15824798-DNA Mutational Analysis, pubmed-meshheading:15824798-Female, pubmed-meshheading:15824798-Genetic Counseling, pubmed-meshheading:15824798-Genetic Testing, pubmed-meshheading:15824798-Humans, pubmed-meshheading:15824798-Male, pubmed-meshheading:15824798-Middle Aged, pubmed-meshheading:15824798-Mutation, pubmed-meshheading:15824798-Myotonic Dystrophy, pubmed-meshheading:15824798-Polymerase Chain Reaction
pubmed:articleTitle	[Myotonic dystrophy type 1 in cataract patients: molecular diagnosis for screening and genetic counseling].
pubmed:affiliation	Departamento de Patologia, Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. veronicamunoz@terra.com.br
pubmed:publicationType	Journal Article, English Abstract, Research Support, Non-U.S. Gov't