Detalhe da pesquisa
1.
Novel clinical and molecular findings in Spanish patients with naevoid basal cell carcinoma syndrome.
Br J Dermatol
; 178(1): 198-206, 2018 01.
Artigo
Inglês
| MEDLINE | ID: mdl-28733979
2.
Almost 2% of Spanish breast cancer families are associated to germline pathogenic mutations in the ATM gene.
Breast Cancer Res Treat
; 161(3): 597-604, 2017 02.
Artigo
Inglês
| MEDLINE | ID: mdl-27913932
3.
Impact of chemotherapy on telomere length in sporadic and familial breast cancer patients.
Breast Cancer Res Treat
; 149(2): 385-94, 2015 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-25528024
4.
Comment on: Clinicopathological features and oncological outcomes of patients with young-onset rectal cancer.
Br J Surg
; 107(8): e277, 2020 07.
Artigo
Inglês
| MEDLINE | ID: mdl-32424850
5.
DNA copy number profiling reveals extensive genomic loss in hereditary BRCA1 and BRCA2 ovarian carcinomas.
Br J Cancer
; 108(8): 1732-42, 2013 Apr 30.
Artigo
Inglês
| MEDLINE | ID: mdl-23558894
6.
Apparent regional differences in the spectrum of BARD1 pathogenic variants in Spanish population and importance of copy number variants.
Sci Rep
; 12(1): 8547, 2022 05 20.
Artigo
Inglês
| MEDLINE | ID: mdl-35595798
7.
Clinical and genetic characterization of classical forms of familial adenomatous polyposis: a Spanish population study.
Ann Oncol
; 22(4): 903-909, 2011 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-20924072
8.
Surgical management of hereditary colorectal cancer: surgery based on molecular analysis and family history.
Rev Esp Enferm Dig
; 101(8): 536-40, 2009 Aug.
Artigo
Inglês
| MEDLINE | ID: mdl-19785492
9.
Chromosome 4p16 and osteochondroplasias.
Nat Genet
; 6(4): 334, 1994 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-8054971
10.
A haplotype containing the p53 polymorphisms Ins16bp and Arg72Pro modifies cancer risk in BRCA2 mutation carriers.
Hum Mutat
; 27(3): 242-8, 2006 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-16419081
11.
Analysis of the INK4a/ARF locus in non-Hodgkin's lymphomas using two new internal microsatellite markers.
Leukemia
; 13(5): 808-10, 1999 May.
Artigo
Inglês
| MEDLINE | ID: mdl-10374887
12.
Chromosomal changes pattern and gene amplification in T cell non-Hodgkin's lymphomas.
Leukemia
; 15(10): 1627-32, 2001 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-11587222
13.
Importance of family history in colorectal cancer clinical practice.
Colorectal Dis
; 12(6): 606, 2010 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-20105203
14.
SMAD4 in early onset colorectal cancer.
Colorectal Dis
; 12(9): 948, 2010 Sep.
Artigo
Inglês
| MEDLINE | ID: mdl-20456468
15.
Genome-wide linkage analysis and tumoral characterization reveal heterogeneity in familial colorectal cancer type X.
J Gastroenterol
; 50(6): 657-66, 2015 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-25381643
16.
Chromosome cultures from human cartilage.
Am J Med Genet
; 46(2): 123-5, 1993 Apr 15.
Artigo
Inglês
| MEDLINE | ID: mdl-8484396
17.
Anencephaly and faciocranioschisis: evidence of complete failure of closure 3 of the neural tube in humans.
Am J Med Genet
; 75(1): 4-6, 1998 Jan 06.
Artigo
Inglês
| MEDLINE | ID: mdl-9450848
18.
Segmentation anomalies of the vertebras and ribs: a developmental field defect: epidemiologic evidence.
Am J Med Genet
; 49(1): 36-44, 1994 Jan 01.
Artigo
Inglês
| MEDLINE | ID: mdl-8172249
19.
DK-phocomelia syndrome in a child with a long follow-up.
Am J Med Genet
; 52(3): 269-71, 1994 Sep 01.
Artigo
Inglês
| MEDLINE | ID: mdl-7810557
20.
New acrofacial dysostosis syndrome in 3 sibs.
Am J Med Genet
; 35(4): 484-9, 1990 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-2333875