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MLH1 Ile219Val Polymorphism in Argentinean Families with Suspected Lynch Syndrome.
Front Oncol. 2016 Aug 24;6:189. doi: 10.3389/fonc.2016.00189. eCollection 2016.
Front Oncol. 2016.
PMID: 27606285
Free PMC article.
No abstract available.
[Founder mutation in Lynch syndrome].
Cajal AR, Piñero TA, Verzura A, Santino JP, Solano AR, Kalfayan PG, Ferro A, Vaccaro C.
Cajal AR, et al.
Medicina (B Aires). 2016;76(3):180-2.
Medicina (B Aires). 2016.
PMID: 27295708
Free article.
Spanish.
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Universal determination of microsatellite instability using BAT26 as a single marker in an Argentine colorectal cancer cohort.
González ML, Causada-Calo N, Santino JP, Dominguez-Valentin M, Ferro FA, Sammartino I, Kalfayan PG, Verzura MA, Piñero TA, Cajal AR, Pavicic W, Vaccaro C.
González ML, et al. Among authors: cajal ar.
Fam Cancer. 2018 Jul;17(3):395-402. doi: 10.1007/s10689-017-0052-4.
Fam Cancer. 2018.
PMID: 29128931
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Maternal ancestry and hematological cancer risk: case-control study in an Argentinean population.
Cerliani MB, Mayordomo AC, Sanchez Dova A, Soarez JN, Fuhr Etcheverry J, Piñero TA, Cajal AR, Jauk F, García-Rivello H, Vaccaro CA, Richard SM, Bravi CM, Pavicic WH.
Cerliani MB, et al. Among authors: cajal ar.
Per Med. 2021 May;18(3):269-281. doi: 10.2217/pme-2020-0062. Epub 2021 Mar 17.
Per Med. 2021.
PMID: 33728969
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Evidence for interaction between markers in GABA(A) receptor subunit genes in an Argentinean autism spectrum disorder population.
Sesarini CV, Costa L, Naymark M, Grañana N, Cajal AR, García Coto M, Pallia RC, Argibay PF.
Sesarini CV, et al. Among authors: cajal ar.
Autism Res. 2014 Feb;7(1):162-6. doi: 10.1002/aur.1353. Epub 2013 Nov 18.
Autism Res. 2014.
PMID: 24249596
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Influence of 5-HTTLPR and 5-HTTVNTR polymorphisms of the serotonin transporter gene (SLC6A4) on major depressive disorder in a sample of Argentinean population.
Cajal AR, Redal MA, Costa LD, Lesik LA, Faccioli JL, Finkelsztein CA, Argibay PF.
Cajal AR, et al.
Psychiatr Genet. 2012 Apr;22(2):103-4. doi: 10.1097/YPG.0b013e32834acc9b.
Psychiatr Genet. 2012.
PMID: 21862951
No abstract available.
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Prevalence of CYP2B6 polymorphisms in Argentinians: the role of genetic testing.
Scibona P, Vazquez C, Cajal AR, Argibay PF, Belloso WH.
Scibona P, et al. Among authors: cajal ar.
Genet Mol Res. 2015 Dec 11;14(4):16594-9. doi: 10.4238/2015.December.11.6.
Genet Mol Res. 2015.
PMID: 26681005
Free article.
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Prevalence of Intracranial Aneurysms in Hereditary Hemorrhagic Telangiectasia: Report from a Single Reference Center.
Perez Akly MS, Vazquez C, Besada CH, Rodriguez MJ, Conde MF, Cajal AR, Peuchot VA, Dardik D, Baccanelli MM, Serra MM.
Perez Akly MS, et al. Among authors: cajal ar.
AJNR Am J Neuroradiol. 2022 Jun;43(6):844-849. doi: 10.3174/ajnr.A7505. Epub 2022 May 19.
AJNR Am J Neuroradiol. 2022.
PMID: 35589139
Free PMC article.
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