Browsing by Author Cantu, JM

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A novel Leu171Pro mutation in presenilin-1 gene in a Mexican family with early onset Alzheimer diseaseRamirez-Duenas, MG; Rogaeva, EA; Leal, CA; Lin, C; Ramirez-Casillas, GA; Hernandez-Romo, JA; St George-Hyslop, PH; Cantu, JM--
A novel Leu171Pro mutation in presenilin-1 gene in a Mexican family with early onset Alzheimer diseaseRamirez-Duenas, MG; Rogaeva, EA; Leal, CA; Lin, C; Ramirez-Casillas, GA; Hernandez-Romo, JA; St George-Hyslop, PH; Cantu, JM--
Are hypotrichosis simplex and monilethrix allelle forms?: Description of a Mexican family.Davalos, N; Davalos, IP; Patino-Garcia, B; Garcia-Vargas, A; Tarango-Martinez, V; Sanchez-Castellanos, ME; Villarreal, I; Garcia-Cruz, D; Feria-Velazco, A; Cantu, JM; Figuera, LE--
Are hypotrichosis simplex and monilethrix allelle forms?: Description of a Mexican family.Davalos, N; Davalos, IP; Patino-García, B; García-Vargas, A; Tarango-Martinez, V; Sanchez-Castellanos, ME; Villarreal, I; García-Cruz, D; Feria-Velazco, A; Cantu, JM; Figuera, LE--
beta(A) globin gene haplotypes in Mexican Huichols: Genetic relatedness to other populationsVillalobos-Arambula, AR; Rivas, F; Sandoval, L; Perea, FJ; Casas-Castaneda, M; Cantu, JM; Ibarra, B--
beta(A) globin gene haplotypes in Mexican Huichols: Genetic relatedness to other populationsVillalobos-Arambula, AR; Rivas, F; Sandoval, L; Perea, FJ; Casas-Castaneda, M; Cantu, JM; Ibarra, B--
(CAG)nCAA and GGN repeats in the human androgen receptor gene are not associated with prostate cancer in a French-German populationCorrea-Cerro, L; Wohr, G; Haussler, J; Berthon, P; Drelon, E; Mangin, P; Fournier, G; Cussenot, O; Kraus, P; Just, W; Paiss, T; Cantu, JM; Vogel, W--
(CAG)nCAA and GGN repeats in the human androgen receptor gene are not associated with prostate cancer in a French-German populationCorrea-Cerro, L; Wohr, G; Haussler, J; Berthon, P; Drelon, E; Mangin, P; Fournier, G; Cussenot, O; Kraus, P; Just, W; Paiss, T; Cantu, JM; Vogel, W--
Familial iridogoniodysgenesis and skeletal anomalies: a probable new autosomal recessive disorderRodriguez-Rojas, LX; Garcia-Cruz, D; Mendoza-Topete, R; Barba, LB; Barrios, MT; Patino-Garcia, B; Lopez-Cardona, MG; Nuno-Arana, I; Garcia-Ortiz, JE; Cantu, JM--
Familial iridogoniodysgenesis and skeletal anomalies: a probable new autosomal recessive disorderRodriguez-Rojas, LX; Garcia-Cruz, D; Mendoza-Topete, R; Barba, LB; Barrios, MT; Patino-Garcia, B; Lopez-Cardona, MG; Nuno-Arana, I; Garcia-Ortiz, JE; Cantu, JM--
Gcn4 participates in the nitrogen discrimination pathway in Saccharomyces cerevisiaeGonzalez, A; Riego, L; Sosa, E; Aranda, C; Valenzuela, L; DeLuna, A; Cantu, JM--
Gcn4 participates in the nitrogen discrimination pathway in Saccharomyces cerevisiaeGonzalez, A; Riego, L; Sosa, E; Aranda, C; Valenzuela, L; DeLuna, A; Cantu, JM--
Genetic variation among four Mexican populations (Huichol, Purepecha, Tarahumara, and Mestizo) revealed by two VNTRs and four STRsRangel-Villalobos, H; Rivas, F; Sandoval, L; Ibarra, B; García-Carvajal, ZY; Cantu, JM; Figuera, LE--
Genetic variation among four Mexican populations (Huichol, Purepecha, Tarahumara, and Mestizo) revealed by two VNTRs and four STRsRangel-Villalobos, H; Rivas, F; Sandoval, L; Ibarra, B; Garcia-Carvajal, ZY; Cantu, JM; Figuera, LE--
Heteroallelic monozygotic twins and tripletsCantu, JM; Diaz-Gallardo, MY; Barros-Nunez, P; Figuera, LE--
Heteroallelic monozygotic twins and tripletsCantu, JM; Diaz-Gallardo, MY; Barros-Nunez, P; Figuera, LE--
Inherited hypertrichosesGarcia-Cruz, D; Figuera, LE; Cantu, JM--
Inherited hypertrichosesGarcía-Cruz, D; Figuera, LE; Cantu, JM--
MTHFR C677T mutation in parents of children with neural tube defects and in normal mestizo and native Mexican populations.Davalos, IP; Olivares, N; Castillo, MT; Cantu, JM; Sandoval, L; Moran-Moguel, MC; Chakraborty, R; Rivas, F--
MTHFR C677T mutation in parents of children with neural tube defects and in normal mestizo and native Mexican populations.Davalos, IP; Olivares, N; Castillo, MT; Cantu, JM; Sandoval, L; Moran-Moguel, MC; Chakraborty, R; Rivas, F--