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FANCC Dutch founder mutation in a Mennonite family from Tamaulipas, México.
García-de Teresa B, Frias S, Molina B, Villarreal MT, Rodriguez A, Carnevale A, López-Hernández G, Vollbrechtshausen L, Olaya-Vargas A, Torres L. García-de Teresa B, et al. Among authors: carnevale a. 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.
Genomic study of dilated cardiomyopathy in a group of Mexican patients using site-directed next generation sequencing.
Carnevale A, Rosas-Madrigal S, Rosendo-Gutiérrez R, López-Mora E, Romero-Hidalgo S, Avila-Vazzini N, Jacobo-Albavera L, Domínguez-Pérez M, Vargas-Alarcón G, Pérez-Villatoro F, Navarrete-Martínez JI, Villarreal-Molina MT. Carnevale A, et al. Mol Genet Genomic Med. 2020 Nov;8(11):e1504. doi: 10.1002/mgg3.1504. Epub 2020 Sep 24. Mol Genet Genomic Med. 2020. PMID: 32969603 Free PMC article.
Low bone mineral density and renal malformation in Mexican patients with Turner syndrome are associated with single nucleotide variants in vitamin D-metabolism genes.
Barrientos-Rios R, Frias S, Velázquez-Aragón JA, Villaroel CE, Sánchez S, Molina B, Martínez A, Carnevale A, García-de-Teresa B, Bonilla E, Alvarado-Araiza CD, Valderrama-Hernández A, Ríos-Gallardo PT, Calzada-León R, Altamirano-Bustamante N, Torres L. Barrientos-Rios R, et al. Among authors: carnevale a. Gynecol Endocrinol. 2019 Sep;35(9):772-776. doi: 10.1080/09513590.2019.1582626. Epub 2019 Mar 19. Gynecol Endocrinol. 2019. PMID: 30887870
332 results