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The LOVD3 platform: efficient genome-wide sharing of genetic variants.
Fokkema IFAC, Kroon M, López Hernández JA, Asscheman D, Lugtenburg I, Hoogenboom J, den Dunnen JT. Fokkema IFAC, et al. Among authors: lopez hernandez ja. Eur J Hum Genet. 2021 Dec;29(12):1796-1803. doi: 10.1038/s41431-021-00959-x. Epub 2021 Sep 15. Eur J Hum Genet. 2021. PMID: 34521998 Free PMC article.
Genetic analysis of muscular dystrophies: our experience in Mexico.
Escobar-Cedillo RE, López-Hernández L, Miranda-Duarte A, Curiel-Leal MD, Suarez-Ocón A, Sánchez-Chapul L, Berenice Luna-Angulo A, Ávila-Ramírez G, López-Hernández JA, Gómez-Díaz B. Escobar-Cedillo RE, et al. Among authors: lopez hernandez ja. Folia Neuropathol. 2021;59(3):276-283. doi: 10.5114/fn.2021.109426. Folia Neuropathol. 2021. PMID: 34628793 Free article.
Comparison of mutation profiles in the Duchenne muscular dystrophy gene among populations: implications for potential molecular therapies.
López-Hernández LB, Gómez-Díaz B, Luna-Angulo AB, Anaya-Segura M, Bunyan DJ, Zúñiga-Guzman C, Escobar-Cedillo RE, Roque-Ramírez B, Ruano-Calderón LA, Rangel-Villalobos H, López-Hernández JA, Estrada-Mena FJ, García S, Coral-Vázquez RM. López-Hernández LB, et al. Among authors: lopez hernandez ja. Int J Mol Sci. 2015 Mar 9;16(3):5334-46. doi: 10.3390/ijms16035334. Int J Mol Sci. 2015. PMID: 25761239 Free PMC article.
Duchenne muscular dystrophy in a developing country: challenges in management and genetic counseling.
López-Hernández LB, Gómez-Díaz B, Escobar-Cedillo RE, Gama-Moreno O, Camacho-Molina A, Soto-Valdés DM, Anaya-Segura MA, Luna-Padrón E, Zúñiga-Guzmán C, Lopez-Hernández JA, Vázquez-Cárdenas NA, Sánchez-Chapul L, Rangel-Villalobos H, Canto P, López-Cardona MG, García S, Méndez-Covarrubias G, Coral-Vázquez RM. López-Hernández LB, et al. Among authors: lopez hernandez ja. Genet Couns. 2014;25(2):129-41. Genet Couns. 2014. PMID: 25059011