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ABCA4 mutational spectrum in Mexican patients with Stargardt disease: Identification of 12 novel mutations and evidence of a founder effect for the common p.A1773V mutation.
Exp Eye Res. 2013 Apr;109:77-82. doi: 10.1016/j.exer.2013.02.006. Epub 2013 Feb 16.
Exp Eye Res. 2013.
PMID: 23419329
Expansion of the clinical ocular spectrum of Wolfram Syndrome in a family carrying a novel WFS1 gene deletion.
Chacón-Camacho O, Arce-Gonzalez R, Granillo-Alvarez M, Flores-Limas S, Ramírez M, Zenteno JC.
Chacón-Camacho O, et al. Among authors: granillo alvarez m.
Ophthalmic Genet. 2013 Dec;34(4):243-8. doi: 10.3109/13816810.2012.755631. Epub 2013 Feb 1.
Ophthalmic Genet. 2013.
PMID: 23373429
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Identification and expression analysis of a novel intragenic EFNB1 mutation causing craniofrontonasal syndrome.
Chacon-Camacho OF, Arce-Gonzalez R, Villegas-Ruiz V, Pelcastre-Luna E, Uría-Gómez CE, Granillo-Alvarez M, Zenteno JC.
Chacon-Camacho OF, et al. Among authors: granillo alvarez m.
Meta Gene. 2013 Nov 28;2:25-31. doi: 10.1016/j.mgene.2013.11.001. eCollection 2014 Dec.
Meta Gene. 2013.
PMID: 25606386
Free PMC article.
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p63 gene analysis in Mexican patients with syndromic and non-syndromic ectrodactyly.
Berdón-Zapata V, Granillo-Alvarez M, Valdés-Flores M, García-Ortiz JE, Kofman-Alfaro S, Zenteno JC.
Berdón-Zapata V, et al. Among authors: granillo alvarez m.
J Orthop Res. 2004 Jan;22(1):1-5. doi: 10.1016/S0736-0266(03)00166-9.
J Orthop Res. 2004.
PMID: 14656652
Free article.
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