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Cystathionine β-synthase and methylenetetrahydrofolate reductase mutations in Mexican individuals with hyperhomocysteinemia.
Figueroa-Torres AG, Matias-Aguilar LO, Coria-Ramirez E, Bonilla-Gonzalez E, Gonzalez-Marquez H, Ibarra-Gonzalez I, Hernandez-Lopez JR, Hernandez-Juarez J, Dominguez-Reyes VM, Isordia-Salas I, Majluf-Cruz A. Figueroa-Torres AG, et al. Among authors: dominguez reyes vm. SAGE Open Med. 2020 Nov 20;8:2050312120974193. doi: 10.1177/2050312120974193. eCollection 2020. SAGE Open Med. 2020. PMID: 33282308 Free PMC article.
von Willebrand Disease and other hereditary haemostatic factor deficiencies in women with a history of postpartum haemorrhage.
Majluf-Cruz K, Anguiano-Robledo L, Calzada-Mendoza CC, Hernández-Juárez J, Moreno-Hernández M, Domínguez-Reyes VM, Figueroa-Torres AG, Gomez-Rosas P, Arreola-Diaz R, García-Lee MT, Ricardo-Moreno MT, Sosa-Camas RE, Garcia-Chavez J, Vela Ojeda J, Isordia-Salas I, Majluf-Cruz A. Majluf-Cruz K, et al. Among authors: dominguez reyes vm. Haemophilia. 2020 Jan;26(1):97-105. doi: 10.1111/hae.13900. Epub 2019 Dec 11. Haemophilia. 2020. PMID: 31823446