Orozco L - Search Results

1

Spectrum of RB1 gene mutations and loss of heterozygosity in Mexican patients with retinoblastoma: identification of six novel mutations.

Macías M, Dean M, Atkinson A, Jiménez-Morales S, García-Vazquez FJ, Saldaña-Alvarez Y, Ramírez-Bello J, Chávez M, Orozco L. Macías M, et al. Among authors: orozco l. Cancer Biomark. 2008;4(2):93-9. doi: 10.3233/cbm-2008-4205. Cancer Biomark. 2008. PMID: 18503160

2

Mild cystic fibrosis disease in three Mexican delta-F508/G551S compound heterozygous siblings.

Orozco L, Lezana JL, Villarreal MT, Chávez M, Carnevale A. Orozco L, et al. Clin Genet. 1995 Feb;47(2):96-8. doi: 10.1111/j.1399-0004.1995.tb03931.x. Clin Genet. 1995. PMID: 7606851

3

[A molecular study of the delta-F508 mutation and genetic analysis of a sample of cystic fibrosis patients].

Orozco L, Lezana JL, Chávez M, Valdez H, Moreno M, Carnevale A. Orozco L, et al. Bol Med Hosp Infant Mex. 1993 Jul;50(7):457-62. Bol Med Hosp Infant Mex. 1993. PMID: 7689846 Spanish.

4

Identification of the I507 deletion by site-directed mutagenesis.

Orozco L, Friedman K, Chávez M, Lezana JL, Villarreal MT, Carnevale A. Orozco L, et al. Am J Med Genet. 1994 Jun 1;51(2):137-9. doi: 10.1002/ajmg.1320510210. Am J Med Genet. 1994. PMID: 8092189

5

Frequency of delta F508 in a Mexican sample of cystic fibrosis patients.

Orozco L, Salcedo M, Lezana JL, Chávez M, Valdez H, Moreno M, Carnevale A. Orozco L, et al. J Med Genet. 1993 Jun;30(6):501-2. doi: 10.1136/jmg.30.6.501. J Med Genet. 1993. PMID: 8326494 Free PMC article.

6

Detection of the cystic fibrosis delta-F508 mutation at autopsy by site-directed mutagenesis.

Salcedo M, Chávez M, Ridaura C, Moreno M, Lezana JL, Orozco L. Salcedo M, et al. Among authors: orozco l. Am J Med Genet. 1993 May 15;46(3):268-70. doi: 10.1002/ajmg.1320460305. Am J Med Genet. 1993. PMID: 8488869

7

G542X mutation in Mexican cystic fibrosis patients.

Villarreal MT, Chávez M, Lezana JL, Cuevas F, Carnevale A, Códova E, del Angel RM, Orozco L. Villarreal MT, et al. Among authors: orozco l. Clin Genet. 1996 Jan;49(1):54-6. doi: 10.1111/j.1399-0004.1996.tb04326.x. Clin Genet. 1996. PMID: 8721574

8

High frequency of de novo deletions in Mexican Duchenne and Becker muscular dystrophy patients. Implications for genetic counseling.

Alcántara MA, Villarreal MT, Del Castillo V, Gutiérrez G, Saldaña Y, Maulen I, Lee R, Macías M, Orozco L. Alcántara MA, et al. Among authors: orozco l. Clin Genet. 1999 May;55(5):376-80. doi: 10.1034/j.1399-0004.1999.550514.x. Clin Genet. 1999. PMID: 10422811

9

Spectrum of CFTR mutations in Mexican cystic fibrosis patients: identification of five novel mutations (W1098C, 846delT, P750L, 4160insGGGG and 297-1G-->A).

Orozco L, Velázquez R, Zielenski J, Tsui LC, Chávez M, Lezana JL, Saldaña Y, Hernández E, Carnevale A. Orozco L, et al. Hum Genet. 2000 Mar;106(3):360-5. doi: 10.1007/s004390051051. Hum Genet. 2000. PMID: 10798368

10

Molecular diagnosis of the fragile X and FRAXE syndromes in patients with mental retardation of unknown cause in Mexico.

González-del Angel A, Vidal S, Saldaña Y, del Castillo V, Angel Alcántara M, Macías M, Pedro Luna J, Orozco L. González-del Angel A, et al. Among authors: orozco l. Ann Genet. 2000 Jan-Mar;43(1):29-34. doi: 10.1016/s0003-3995(00)00018-6. Ann Genet. 2000. PMID: 10818218

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