A non-sense mutation in the corneodesmosin gene in a Mexican family with hypotrichosis simplex of the scalp
Dávalos, N.O., García-Vargas, A., Pforr, J., Dávalos, I.P., Picos-Cárdenas, V.J., García-Cruz, D., Kruse, R., Figuera, L.E., Nöthen, M.M., Betz, R.C.
Published in British journal of dermatology (1951) (01.12.2005)
Published in British journal of dermatology (1951) (01.12.2005)
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IDF23-0531 Genetic variants of AGER gene and its association with renal function in type 2 diabetes Mexican patients
Diaz, L. Delgado, Barraza, J. Camberos, Alvarez, E.E. Alvarez, Zamora, L. Calderón, Rojo, C.E. Angulo, Gómez, J.A. Magaña, De la Herrán-Arita, A.K., Flores, M.A. Valdez, Ramos, J.F. Osuna, Cárdenas, V.J. Picos, Valenzuela, C.D. Norzagaray, Llanos, A.M. Guadrón
Published in Diabetes research and clinical practice (01.03.2024)
Published in Diabetes research and clinical practice (01.03.2024)
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eNOS gene Glu298Asp and 4b/a polymorphisms are associated with renal function parameters in Mexican patients with Fabry disease
Marin-Medina, A, Brambila-Tapia, A J L, Picos-Cárdenas, V J, Gallegos-Arreola, M P, Figuera, L E
Published in Genetics and molecular research (24.10.2016)
Published in Genetics and molecular research (24.10.2016)
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Calpain-10 gene polymorphisms and risk of type 2 diabetes mellitus in Mexican mestizos
Picos-Cárdenas, V J, Sáinz-González, E, Miliar-García, A, Romero-Zazueta, A, Quintero-Osuna, R, Leal-Ugarte, E, Peralta-Leal, V, Meza-Espinoza, J P
Published in Genetics and molecular research (27.03.2015)
Published in Genetics and molecular research (27.03.2015)
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Paternal isodisomy 7q secondary to monosomy 7 at recurrence in a Down syndrome child with acute myelogenous leukemia
Picos-Cárdenas, V.J., Meza-Espinoza, J.P., Gutiérrez-Angulo, M., Esparza-Flores, M.A., Ayala-Madrigal, M.L., Hansmann, I., González, G.J.R.
Published in Cancer genetics and cytogenetics (15.04.2002)
Published in Cancer genetics and cytogenetics (15.04.2002)
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