Blanco I - Search Results

1

Founder mutation in familial adenomatous polyposis (FAP) in the Balearic Islands.

González S, Blanco I, Campos O, Julià M, Reyes J, Llompart A, Cabeza E, Germà JR, Obrador A, Capellá G. González S, et al. Among authors: blanco i. Cancer Genet Cytogenet. 2005 Apr 1;158(1):70-4. doi: 10.1016/j.cancergencyto.2004.07.003. Cancer Genet Cytogenet. 2005. PMID: 15771908

2

Germline hypermethylation of the APC promoter is not a frequent cause of familial adenomatous polyposis in APC/MUTYH mutation negative families.

Romero-Giménez J, Dopeso H, Blanco I, Guerra-Moreno A, Gonzalez S, Vogt S, Aretz S, Schwartz S Jr, Capella G, Arango D. Romero-Giménez J, et al. Among authors: blanco i. Int J Cancer. 2008 Mar 15;122(6):1422-5. doi: 10.1002/ijc.23247. Int J Cancer. 2008. PMID: 18027849

3

Founder effect of a pathogenic MSH2 mutation identified in Spanish families with Lynch syndrome.

Menéndez M, Castellví-Bel S, Pineda M, de Cid R, Muñoz J, González S, Teulé A, Balaguer F, Ramón y Cajal T, Reñé JM, Blanco I, Castells A, Capellà G. Menéndez M, et al. Among authors: blanco i. Clin Genet. 2010 Aug;78(2):186-90. doi: 10.1111/j.1399-0004.2009.01346.x. Epub 2010 Jan 20. Clin Genet. 2010. PMID: 20095990

4

Functional characterization of the novel APC N1026S variant associated with attenuated familial adenomatous polyposis.

Menéndez M, González S, Obrador-Hevia A, Domínguez A, Pujol MJ, Valls J, Canela N, Blanco I, Torres A, Pineda-Lucena A, Moreno V, Bachs O, Capellá G. Menéndez M, et al. Among authors: blanco i. Gastroenterology. 2008 Jan;134(1):56-64. doi: 10.1053/j.gastro.2007.10.009. Epub 2007 Oct 10. Gastroenterology. 2008. PMID: 18166348

5

Detection of APC gene deletions using quantitative multiplex PCR of short fluorescent fragments.

Castellsagué E, González S, Nadal M, Campos O, Guinó E, Urioste M, Blanco I, Frebourg T, Capellá G. Castellsagué E, et al. Among authors: blanco i. Clin Chem. 2008 Jul;54(7):1132-40. doi: 10.1373/clinchem.2007.101006. Epub 2008 May 16. Clin Chem. 2008. PMID: 18487285

6

Clinical and genetic characterization of classical forms of familial adenomatous polyposis: a Spanish population study.

Rivera B, González S, Sánchez-Tomé E, Blanco I, Mercadillo F, Letón R, Benítez J, Robledo M, Capellá G, Urioste M. Rivera B, et al. Among authors: blanco i. Ann Oncol. 2011 Apr;22(4):903-909. doi: 10.1093/annonc/mdq465. Epub 2010 Oct 5. Ann Oncol. 2011. PMID: 20924072 Free article.

7

[Familial adenomatous polyposis].

Parés D, Pera M, González S, Pascual Cruz M, Blanco I. Parés D, et al. Among authors: blanco i. Gastroenterol Hepatol. 2006 Dec;29(10):625-35. doi: 10.1157/13095198. Gastroenterol Hepatol. 2006. PMID: 17198641 Review. Spanish.

8

Identification of a founder EPCAM deletion in Spanish Lynch syndrome families.

Mur P, Pineda M, Romero A, Del Valle J, Borràs E, Canal A, Navarro M, Brunet J, Rueda D, Ramón Y Cajal T, Lázaro C, Caldés T, Blanco I, Soto JL, Capellá G. Mur P, et al. Among authors: blanco i. Clin Genet. 2014 Mar;85(3):260-6. doi: 10.1111/cge.12152. Epub 2013 Apr 26. Clin Genet. 2014. PMID: 23530899

9

Polymorphisms in genes of nucleotide and base excision repair: risk and prognosis of colorectal cancer.

Moreno V, Gemignani F, Landi S, Gioia-Patricola L, Chabrier A, Blanco I, González S, Guino E, Capellà G, Canzian F. Moreno V, et al. Among authors: blanco i. Clin Cancer Res. 2006 Apr 1;12(7 Pt 1):2101-8. doi: 10.1158/1078-0432.CCR-05-1363. Clin Cancer Res. 2006. PMID: 16609022

10

Tumor LOH analysis provides reliable linkage information for prenatal genetic testing of sporadic NF1 patients.

Serra E, Pros E, García C, López E, Gili ML, Gómez C, Ravella A, Capellá G, Blanco I, Lázaro C. Serra E, et al. Among authors: blanco i. Genes Chromosomes Cancer. 2007 Sep;46(9):820-7. doi: 10.1002/gcc.20468. Genes Chromosomes Cancer. 2007. PMID: 17563086

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