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Results: 1-4 |
Results: 4

Authors: Orozco, L Gonzalez, L Chavez, M Velazquez, R Lezana, JL Saldana, Y Villarreal, T Carnevale, A
Citation: L. Orozco et al., XV-2c/KM-19 haplotype analysis of cystic fibrosis mutations in Mexican patients, AM J MED G, 102(3), 2001, pp. 277-281

Authors: Orozco, L Velazquez, R Zielenski, J Tsui, LC Chavez, M Lezana, JL Saldana, Y Hernandez, E Carnevale, A
Citation: L. Orozco et al., Spectrum of CFTR mutations in Mexican cystic fibrosis patients: identification of five novel mutations [W1098C, 846delT, P750L, 4160insGGGG and 297-1G -> A), HUM GENET, 106(3), 2000, pp. 360-365

Authors: Gonzalez-del Angel, A Vidal, S Saldana, Y del Castillo, V Alcantara, MA Macias, M Luna, JP Orozco, L
Citation: A. Gonzalez-del Angel et al., Molecular diagnosis of the fragile X and FRAXE syndromes in patients with mental retardation of unknown cause in Mexico, ANN GENET, 43(1), 2000, pp. 29-34

Authors: Alcantara, MA Villarreal, MT Del Castillo, V Gutierrez, G Saldana, Y Maulen, I Lee, R Macias, M Orozco, L
Citation: Ma. Alcantara et al., High frequency of de novo deletions in Mexican Duchenne and Becker muscular dystrophy patients. Implications for genetic counseling, CLIN GENET, 55(5), 1999, pp. 376-380
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