Browsing by Author Arnaud, L

Jump to: 0-9 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
or enter first few letters:  
Showing results 1 to 8 of 8
TitleAuthor(s)???itemlist.dc.contributor.other??????itemlist.dc.contributor.editor???
Association of genetic polimorphysm APOB (VNTR) in patients with isquemic cardiomyopathy of Mexican population.Gallegos, MP; Rangel, H; Zuniga, M; Arnaud, L; Lopez, L; Figuera, LE; Beltran, TJ; Arechavaleta, MR; Sandoval, L; Zuniga, GM--
Association of genetic polimorphysm APOB (VNTR) in patients with isquemic cardiomyopathy of Mexican population.Gallegos, MP; Rangel, H; Zuniga, M; Arnaud, L; Lopez, L; Figuera, LE; Beltran, TJ; Arechavaleta, MR; Sandoval, L; Zuniga, GM--
Frequency of Pvull (LPL) genetic polymorphism in patients with Arterial Coronary Disease from Mexican population.Arnaud, L; Gallegos, MP; Mariaud, RP; Ramirez, LJ; Figuera, LE; Ventura, AJ; Gaxiola, R; Beltran, TJ; Zuniga, GM--
Frequency of Pvull (LPL) genetic polymorphism in patients with Arterial Coronary Disease from Mexican population.Arnaud, L; Gallegos, MP; Mariaud, RP; Ramirez, LJ; Figuera, LE; Ventura, AJ; Gaxiola, R; Beltran, TJ; Zuniga, GM--
Genetic polymorphism of CYP2D6 and lung cancer risk.Arnaud, L; Gallegos, MP; Gomez, BC; Morgan, G; Flores, MC; Rangel, H; Zuiga, GM--
Genetic polymorphism of CYP2D6 and lung cancer risk.Arnaud, L; Gallegos, MP; Gomez, BC; Morgan, G; Flores, MC; Rangel, H; Zuiga, GM--
Infantile Systemic Hyalinosis in a patient with chromosome 22 inversion.Marcias-Gomez, N; Arnaud, L; Nastasi, JA; Duran, J; Gomez-Sanchez, H; Davalos-Pulido, RM; Vasquez, AI; Garcia-Ortiz, JE; Gallegos-Arreola, MP; Figuera, LE--
Infantile Systemic Hyalinosis in a patient with chromosome 22 inversion.Marcias-Gomez, N; Arnaud, L; Nastasi, JA; Duran, J; Gomez-Sanchez, H; Davalos-Pulido, RM; Vasquez, AI; García-Ortiz, JE; Gallegos-Arreola, MP; Figuera, LE--