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