Detalhe da pesquisa
1.
A role of SCN9A in human epilepsies, as a cause of febrile seizures and as a potential modifier of Dravet syndrome.
PLoS Genet
; 5(9): e1000649, 2009 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-19763161
2.
Community engagement and informed consent in the International HapMap project.
Community Genet
; 10(3): 186-98, 2007.
Artigo
em Inglês
| MEDLINE | ID: mdl-17575464
3.
Analytical and Clinical Validity Study of FirstStepDx PLUS: A Chromosomal Microarray Optimized for Patients with Neurodevelopmental Conditions.
PLoS Curr
; 92017 Feb 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-28357155
4.
AGT genetic variation, plasma AGT, and blood pressure: An analysis of the Utah Genetic Reference Project pedigrees.
Am J Hypertens
; 23(8): 917-23, 2010 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-20414195
5.
Further evidence for the role of genes on chromosome 2 and chromosome 5 in the inheritance of pulmonary function.
Am J Respir Crit Care Med
; 168(5): 556-61, 2003 Sep 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-12791583
6.
Genetic analysis of a complex trait in the Utah Genetic Reference Project: a major locus for PTC taste ability on chromosome 7q and a secondary locus on chromosome 16p.
Hum Genet
; 112(5-6): 567-72, 2003 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-12624758