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Trisomy 1q41-qter and monosomy 3p26.3-pter in a family with a translocation (1;3): further delineation of the syndromes.
Cervantes A, García-Delgado C, Fernández-Ramírez F, Galaz-Montoya C, Morales-Jiménez AB, Nieto-Martínez K, Gómez-Laguna L, Villa-Morales J, Quintana-Palma M, Berúmen J, Kofman S, Morán-Barroso VF. Cervantes A, et al. Among authors: villa morales j. BMC Med Genomics. 2014 Sep 15;7:55. doi: 10.1186/1755-8794-7-55. BMC Med Genomics. 2014. PMID: 25223409 Free PMC article.
Nance-Horan syndrome in females due to a balanced X;1 translocation that disrupts the NHS gene: Familial case report and review of the literature.
Gómez-Laguna L, Martínez-Herrera A, Reyes-de la Rosa ADP, García-Delgado C, Nieto-Martínez K, Fernández-Ramírez F, Valderrama-Atayupanqui TY, Morales-Jiménez AB, Villa-Morales J, Kofman S, Cervantes A, Morán-Barroso VF. Gómez-Laguna L, et al. Among authors: villa morales j. Ophthalmic Genet. 2018 Jan-Feb;39(1):56-62. doi: 10.1080/13816810.2017.1363245. Epub 2017 Sep 18. Ophthalmic Genet. 2018. PMID: 28922055 Review.
Circulating markers of oxidative stress are associated with a muscle injury in patients with muscular dystrophy Duchenne.
Almeida-Becerril T, Rodríguez-Cruz M, Raúl Sánchez-González J, Antonio Villaldama-Soriano M, Atilano-Miguel S, Villa-Morales J, Cárdenas-Conejo A, Cárdenas-Vázquez R. Almeida-Becerril T, et al. Among authors: villa morales j. Brain Dev. 2021 Jan;43(1):111-120. doi: 10.1016/j.braindev.2020.06.013. Epub 2020 Jul 9. Brain Dev. 2021. PMID: 32654955
The muscle regeneration marker FOXP3 is associated with muscle injury in Duchenne muscular dystrophy.
Yannin Hernández-de la Cruz S, Ordaz-Robles T, Antonio Villaldama-Soriano M, Emmanuel Luna-Guzmán C, Almeida-Becerril T, Villa-Morales J, Cárdenas-Conejo A, Dolores Ruíz-Cruz E, Maldonado-Hernandez J, Bernabe-Garcia M, Barbosa-Cortés L, Rodríguez-Cruz M. Yannin Hernández-de la Cruz S, et al. Among authors: villa morales j. Brain Dev. 2024 May;46(5):199-206. doi: 10.1016/j.braindev.2024.02.001. Epub 2024 Feb 22. Brain Dev. 2024. PMID: 38388302 Clinical Trial.