Detalhe da pesquisa
1.
A genome-wide association study on copy-number variation identifies a 11q11 loss as a candidate susceptibility variant for colorectal cancer.
Hum Genet
; 133(5): 525-34, 2014 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-24218287
2.
High incidence of large deletions in the PMS2 gene in Spanish Lynch syndrome families.
Clin Genet
; 85(6): 583-8, 2014 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-23837913
3.
Pharmacogenomics in colorectal cancer: a genome-wide association study to predict toxicity after 5-fluorouracil or FOLFOX administration.
Pharmacogenomics J
; 13(3): 209-17, 2013 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-22310351
4.
A two-phase case-control study for colorectal cancer genetic susceptibility: candidate genes from chromosomal regions 9q22 and 3q22.
Br J Cancer
; 105(6): 870-5, 2011 Sep 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-21811255
5.
COGENT (COlorectal cancer GENeTics): an international consortium to study the role of polymorphic variation on the risk of colorectal cancer.
Br J Cancer
; 102(2): 447-54, 2010 Jan 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-19920828
6.
BMPR1A mutations in early-onset colorectal cancer with mismatch repair proficiency.
Clin Genet
; 84(1): 94-6, 2013 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-23057600
7.
Candidate predisposing germline copy number variants in early onset colorectal cancer patients.
Clin Transl Oncol
; 19(5): 625-632, 2017 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-27888432
8.
Duplication and deletion analysis by fluorescent real-time PCR-based genotyping.
Clin Chim Acta
; 363(1-2): 138-46, 2006 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-16153621
9.
Breast tumor resembling the tall cell variant of papillary thyroid carcinoma: a case report.
Int J Surg Pathol
; 14(1): 79-84, 2006 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-16501842
10.
Report of the fifth meeting of the European Consortium 'Care for CMMRD' (C4CMMRD), Leiden, The Netherlands, July 6th 2019.
Fam Cancer
; 20(1): 67-73, 2021 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32613597
11.
Beyond BRCA1 and BRCA2 wild-type breast and/or ovarian cancer families: germline mutations in TP53 and PTEN.
Clin Genet
; 77(2): 193-6, 2010 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-19930417
12.
Mutation analysis of the adenomatous polyposis coli (APC) gene in northwest Spanish patients with familial adenomatous polyposis (FAP) and sporadic colorectal cancer.
Hum Mutat
; 18(4): 355, 2001 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-11668620
13.
Somatic but not germline mutation of the APC gene in a case of cribriform-morular variant of papillary thyroid carcinoma.
Am J Clin Pathol
; 115(4): 486-93, 2001 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-11293895
14.
[Smith-Magenis syndrome: a report of two new cases and an approximation to their characteristic behavioural phenotype]. / Síndrome de Smith-Magenis: aportación de dos nuevos casos y aproximación a su característico fenotipo conductual.
Rev Neurol
; 38(11): 1038-42, 2004.
Artigo
em Espanhol
| MEDLINE | ID: mdl-15202082
15.
The Asp1822Val variant of the APC gene is a common polymorphism without clinical implications.
J Med Genet
; 38(10): E33, 2001 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-11584047
16.
The Benefit of a Roseobacter Species on the Survival of Scallop Larvae.
Mar Biotechnol (NY)
; 1(1): 52-59, 1999 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-10373610
17.
Roseobacter gallaeciensis sp. nov., a new marine bacterium isolated from rearings and collectors of the scallop Pecten maximus.
Int J Syst Bacteriol
; 48 Pt 2: 537-42, 1998 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-9731295
18.
Rapid real-time fluorescent PCR gene dosage test for the diagnosis of DNA duplications and deletions.
Clin Chem
; 46(10): 1574-82, 2000 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-11017934
19.
Rare HRAS1 alleles are a risk factor for the development of brain tumors.
Cancer
; 92(11): 2920-6, 2001 Dec 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-11753967
20.
Analysis of BRCA1 and BRCA2 in breast and breast/ovarian cancer families shows population substructure in the Iberian peninsula.
Ann Hum Genet
; 66(Pt 1): 29-36, 2002 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-12014998