Results 121 to 130 of about 14,186 (203)

Advantage of using allele-specific copy numbers when testing for association in regions with common copy number variants. [PDF]

PLoS One, 2013
Marenne G, Chanock SJ, Malats N, Génin E.   +3 more
europepmc   +1 more source

Pancreatic cancer risk and levels of trace elements. [PDF]

Gut, 2012
Amaral AF, Porta M, Silverman DT, Milne RL, Kogevinas M, Rothman N, Cantor KP, Jackson BP, Pumarega JA, López T, Carrato A, Guarner L, Real FX, Malats N.   +13 more
europepmc   +1 more source

Fundamentación gnoseológica de la ética escéptica [PDF]

, 1993
Rodríguez Donís, Marcelino
core  

[Freedom of management: our last chance?]. [PDF]

Aten Primaria, 2011
Coll Benejam JM, Grupo de Trabajo de Autonomía de Gestión.   +1 more
europepmc   +1 more source

The UBC-40 Urothelial Bladder Cancer cell line index: a genomic resource for functional studies. [PDF]

BMC Genomics, 2015
Earl J, Rico D, Carrillo-de-Santa-Pau E, Rodríguez-Santiago B, Méndez-Pertuz M, Auer H, Gómez G, Grossman HB, Pisano DG, Schulz WA, Pérez-Jurado LA, Carrato A, Theodorescu D, Chanock S, Valencia A, Real FX.   +15 more
europepmc   +1 more source

Novel genes involved in severe early-onset obesity revealed by rare copy number and sequence variants. [PDF]

PLoS Genet, 2017
Serra-Juhé C, Martos-Moreno GÁ, Bou de Pieri F, Flores R, González JR, Rodríguez-Santiago B, Argente J, Pérez-Jurado LA.   +7 more
europepmc   +1 more source

Mosaic uniparental disomies and aneuploidies as large structural variants of the human genome. [PDF]

Am J Hum Genet, 2010
Rodríguez-Santiago B, Malats N, Rothman N, Armengol L, Garcia-Closas M, Kogevinas M, Villa O, Hutchinson A, Earl J, Marenne G, Jacobs K, Rico D, Tardón A, Carrato A, Thomas G, Valencia A, Silverman D, Real FX, Chanock SJ, Pérez-Jurado LA.   +19 more
europepmc   +1 more source

Sobre la muerte y el alma separada [PDF]

, 1980
Saranyana, J.I. (Josep Ignasi)
core  

Concentrations of trace elements and KRAS mutations in pancreatic ductal adenocarcinoma. [PDF]

Environ Mol Mutagen, 2019
Gómez-Tomás Á, Pumarega J, Alguacil J, Amaral AFS, Malats N, Pallarès N, Gasull M, Porta M, PANKRAS II Study Group.   +8 more
europepmc   +1 more source

Contribution of rare copy number variants to isolated human malformations. [PDF]

PLoS One, 2012
Serra-Juhé C, Rodríguez-Santiago B, Cuscó I, Vendrell T, Camats N, Torán N, Pérez-Jurado LA.   +6 more
europepmc   +1 more source