Detalhe da pesquisa
1.
Genetic variants in the IL1A gene region contribute to intestinal-type gastric carcinoma susceptibility in European populations.
Int J Cancer
; 135(6): 1343-55, 2014 Sep 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-24615437
2.
Genetic association of gastric cancer with miRNA clusters including the cancer-related genes MIR29, MIR25, MIR93 and MIR106: results from the EPIC-EURGAST study.
Int J Cancer
; 135(9): 2065-76, 2014 Nov 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-24643999
3.
Prediagnostic telomere length and risk of B-cell lymphoma-Results from the EPIC cohort study.
Int J Cancer
; 135(12): 2910-7, 2014 Dec 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-24771230
4.
Correlation between SMA type and SMN2 copy number revisited: An analysis of 625 unrelated Spanish patients and a compilation of 2834 reported cases.
Neuromuscul Disord
; 28(3): 208-215, 2018 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-29433793
5.
Marker and real-time quantitative analyses to confirm hemophilia B carrier diagnosis of a complete deletion of the F9 gene.
Haematologica
; 92(11): 1583-4, 2007 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-18024414
6.
Rapid identification of female haemophilia A carriers with deletions in the factor VIII gene by quantitative real-time PCR analysis.
Thromb Haemost
; 94(3): 661-4, 2005 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-16268486
7.
First report of two independent point factorVIII mutations in a family with haemophilia a: a word of caution for carrier diagnosis.
Thromb Haemost
; 94(3): 675-7, 2005 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-16268489
8.
Clinical and genetic findings in five female patients with haemophilia A: Identification of a novel missense mutation, p.Phe2127Ser.
Thromb Haemost
; 104(4): 718-23, 2010 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-20664893
9.
Identification of 31 novel mutations in the F8 gene in Spanish hemophilia A patients: structural analysis of 20 missense mutations suggests new intermolecular binding sites.
Blood
; 111(7): 3468-78, 2008 Apr 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-18184865