Browsing by Author Duran-Gonzalez, J.

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A de novo interstitial 6q deletion in a boy with a split hand malformationDuran-Gonzalez, J.; Gutierrez-Angulo, M.; Garcia-Cruz, D.; Ayala Ma.D.L.L.; Padilla, M.; Davalos, I.P.--
A de novo interstitial 6q deletion in a boy with a split hand malformationDuran-Gonzalez, J.; Gutierrez-Angulo, M.; Garcia-Cruz, D.; Ayala Ma.D.L.L.; Padilla, M.; Davalos, I.P.--
Association analysis of vitamin D receptor gene polymorphisms and bone mineral density in postmenopausal Mexican-Mestizo womenGonzalez-Mercado, A.; Sanchez-Lopez, J.Y.; Regla-Nava, J.A.; Gamez-Nava, J.I.; Gonzalez-Lopez, L.; Duran-Gonzalez, J.; Celis, A.; Perea-Diaz, F.J.; Salazar-Paramo, M.; Ibarra, B.--
Association analysis of vitamin D receptor gene polymorphisms and bone mineral density in postmenopausal Mexican-Mestizo womenGonzalez-Mercado, A.; Sanchez-Lopez, J.Y.; Regla-Nava, J.A.; Gamez-Nava, J.I.; Gonzalez-Lopez, L.; Duran-Gonzalez, J.; Celis, A.; Perea-Diaz, F.J.; Salazar-Paramo, M.; Ibarra, B.--
Association of a serotonin transporter gene (SLC6A4) 5-HTTLPR polymorphism with body mass index categories but not type 2 diabetes mellitus in MexicansPeralta-Leal, V.; Leal-Ugarte, E.; Meza-Espinoza, J.P.; Davalos-Rodriguez, I.P.; Bocanegra-Alonso, A.; Acosta-Gonzalez, R.I.; Gonzales, E.; Nair, S.; Duran-Gonzalez, J.--
Association of a serotonin transporter gene (SLC6A4) 5-HTTLPR polymorphism with body mass index categories but not type 2 diabetes mellitus in MexicansPeralta-Leal, V.; Leal-Ugarte, E.; Meza-Espinoza, J.P.; Davalos-Rodriguez, I.P.; Bocanegra-Alonso, A.; Acosta-Gonzalez, R.I.; Gonzales, E.; Nair, S.; Duran-Gonzalez, J.--
Association of serotonin transporter gene polymorphism 5-HTTLPR and depressive disorder in a Mexican populationPeralta-Leal, V.; Leal-Ugarte, E.; Meza-Espinoza, J.P.; Gutierrez-Angulo, M.; Hernandez-Benitez, C.T.; Garcia-Rodriguez, A.; Davalos-Rodriguez, I.P.; Gonzales, E.; Duran-Gonzalez, J.--
Association of serotonin transporter gene polymorphism 5-HTTLPR and depressive disorder in a Mexican populationPeralta-Leal, V.; Leal-Ugarte, E.; Meza-Espinoza, J.P.; Gutierrez-Angulo, M.; Hernandez-Benitez, C.T.; García-Rodriguez, A.; Davalos-Rodriguez, I.P.; Gonzales, E.; Duran-Gonzalez, J.--
Benign familial macrocephaly in a mother-son pairDiaz-Rodriguez, M.; Becerra-Solano, L.E.; Toscano-Flores, J.J.; Banuelos-Robles, O.; Duran-Gonzalez, J.; Duenas, M.L.R.--
Benign familial macrocephaly in a mother-son pairDiaz-Rodriguez, M.; Becerra-Solano, L.E.; Toscano-Flores, J.J.; Banuelos-Robles, O.; Duran-Gonzalez, J.; Duenas, M.L.R.--
MDR1 C3435T polymorphism in mexican children with acute lymphoblastic leukemia and in healthy individualsLeal-Ugarte, E.; Gutierrez-Angulo, M.; Macias-gomez, N.M.; Peralta-Leal, V.; Duran-Gonzalez, J.; De La Luz Ayala-Madrigal, M.; Partida-Perez, M.; Barros-Nunez, P.; Ruiz-Diaz, D.; Moreno-Ortiz, J.M.; Peregrina-Sandoval, J.; Meza-Espinoza, J.P.--
MDR1 C3435T polymorphism in mexican children with acute lymphoblastic leukemia and in healthy individualsLeal-Ugarte, E.; Gutierrez-Angulo, M.; Macias-gomez, N.M.; Peralta-Leal, V.; Duran-Gonzalez, J.; De La Luz Ayala-Madrigal, M.; Partida-Perez, M.; Barros-Nunez, P.; Ruiz-Diaz, D.; Moreno-Ortiz, J.M.; Peregrina-Sandoval, J.; Meza-Espinoza, J.P.--
MTHFR C677T, MTHFR A1298C, and OPG A163G polymorphisms in Mexican patients with rheumatoid arthritis and osteoporosisBrambila-Tapia, A.J.L.; Duran-Gonzalez, J.; Sandoval-Ramirez, L.; Mena, J.P.; Salazar-Paramo, M.; Gamez-Nava, J.I.; Gonzalez-Lopez, L.; Lazalde-Medina B, B.; Davalos, N.O.; Peralta-Leal, V.; Del Mercado, M.V.; Beltran-Miranda, C.P.; Davalos, I.P.--
MTHFR C677T, MTHFR A1298C, and OPG A163G polymorphisms in Mexican patients with rheumatoid arthritis and osteoporosisBrambila-Tapia, A.J.L.; Duran-Gonzalez, J.; Sandoval-Ramirez, L.; Mena, J.P.; Salazar-Paramo, M.; Gamez-Nava, J.I.; Gonzalez-Lopez, L.; Lazalde-Medina B, B.; Davalos, N.O.; Peralta-Leal, V.; Del Mercado, M.V.; Beltran-Miranda, C.P.; Davalos, I.P.--
Mutations in the arginine vasopressin neurophysin-II gene in familial neurohypophyseal diabetes insipidus patients [Mutaciones en el gen de arginina vasopresina neurofisina II en pacientes con diabetes insípida neurohipofisiaria familiar]Peralta-Leal, V.; Duran-Gonzalez, J.; Leal-Ugarte, C.E.--
Mutations in the arginine vasopressin neurophysin-II gene in familial neurohypophyseal diabetes insipidus patients [Mutaciones en el gen de arginina vasopresina neurofisina II en pacientes con diabetes insípida neurohipofisiaria familiar]Peralta-Leal, V.; Duran-Gonzalez, J.; Leal-Ugarte, C.E.--
Non-syndromic cleft lip/cleft palate and C677T methylene-tetrahydrofolate reductase variant in Mexican children [Variante C677T del gen metileno-tetrahidrofolato reductasa en niños mexicanos con labio/paladar hendido no sindrómico.]Davalos-Rodriguez, I.P.; Ramirez-Lizardo, E.J.; Mena, J.P.; Ledezma-Rodriguez, V.; Omayra-Davalos, N.; Gonzalez-Mercado, M.G.; Duran-Gonzalez, J.; Moran-Moguel, M.C.; Peralta-Leal, V.; Salazar-Paramo, M.; Ledezma-Gomez, V.--
Non-syndromic cleft lip/cleft palate and C677T methylene-tetrahydrofolate reductase variant in Mexican children [Variante C677T del gen metileno-tetrahidrofolato reductasa en ni�os mexicanos con labio/paladar hendido no sindr�mico.]Davalos-Rodriguez, I.P.; Ramirez-Lizardo, E.J.; Mena, J.P.; Ledezma-Rodriguez, V.; Omayra-Davalos, N.; Gonzalez-Mercado, M.G.; Duran-Gonzalez, J.; Moran-Moguel, M.C.; Peralta-Leal, V.; Salazar-Paramo, M.; Ledezma-Gomez, V.--
Polymorphisms of the XRCC1 gene and breast cancer risk in the Mexican populationMacias-Gomez, N.M.; Peralta-Leal, V.; Meza-Espinoza, J.P.; Gutierrez-Angulo, M.; Duran-Gonzalez, J.; Ramirez-Gonzalez, J.M.; Gaspar-Del Toro, A.; Norberto-Rodriguez, A.; Leal-Ugarte, E.--
Polymorphisms of the XRCC1 gene and breast cancer risk in the Mexican populationMacias-Gomez, N.M.; Peralta-Leal, V.; Meza-Espinoza, J.P.; Gutierrez-Angulo, M.; Duran-Gonzalez, J.; Ramirez-Gonzalez, J.M.; Gaspar-Del Toro, A.; Norberto-Rodriguez, A.; Leal-Ugarte, E.--