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FANCC Dutch founder mutation in a Mennonite family from Tamaulipas, México.
Mol Genet Genomic Med. 2019 Jun;7(6):e710. doi: 10.1002/mgg3.710. Epub 2019 May 1.
Mol Genet Genomic Med. 2019.
PMID: 31044565
Free PMC article.
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. Among authors: villarreal mt.
Clin Genet. 1995 Feb;47(2):96-8. doi: 10.1111/j.1399-0004.1995.tb03931.x.
Clin Genet. 1995.
PMID: 7606851
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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.
Clin Genet. 1996 Jan;49(1):54-6. doi: 10.1111/j.1399-0004.1996.tb04326.x.
Clin Genet. 1996.
PMID: 8721574
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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. Among authors: villarreal mt.
Am J Med Genet. 1994 Jun 1;51(2):137-9. doi: 10.1002/ajmg.1320510210.
Am J Med Genet. 1994.
PMID: 8092189
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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: villarreal mt.
Clin Genet. 1999 May;55(5):376-80. doi: 10.1034/j.1399-0004.1999.550514.x.
Clin Genet. 1999.
PMID: 10422811
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