Detalles de la búsqueda
1.
Increased brain expression of GPNMB is associated with genome wide significant risk for Parkinson's disease on chromosome 7p15.3.
Neurogenetics
; 18(3): 121-133, 2017 Jul.
Artículo
en Inglés
| MEDLINE | ID: mdl-28391543
2.
Impact of copy number variations burden on coding genome in humans using integrated high resolution arrays.
Genet Res (Camb)
; 96: e17, 2014 Dec 16.
Artículo
en Inglés
| MEDLINE | ID: mdl-25578402
3.
High-resolution arrays reveal burden of copy number variations on Parkinson disease genes associated with increased disease risk in random cohorts.
Neurol Res
; 38(9): 775-85, 2016 Sep.
Artículo
en Inglés
| MEDLINE | ID: mdl-27399248
4.
Type 2 diabetes mellitus disease risk genes identified by genome wide copy number variation scan in normal populations.
Diabetes Res Clin Pract
; 113: 160-70, 2016 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-26830856
5.
Copy number variations burden on miRNA genes reveals layers of complexities involved in the regulation of pathways and phenotypic expression.
PLoS One
; 9(2): e90391, 2014.
Artículo
en Inglés
| MEDLINE | ID: mdl-24587348
Resultados
1 -
5
de 5
1
Próxima >
>>