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CDKL5 truncation due to a t(X;2)(p22.1;p25.3) in a girl with X-linked infantile spasm syndrome.
Córdova-Fletes C, Rademacher N, Müller I, Mundo-Ayala JN, Morales-Jeanhs EA, García-Ortiz JE, León-Gil A, Rivera H, Domínguez MG, Kalscheuer VM. Córdova-Fletes C, et al. Among authors: mundo ayala jn. Clin Genet. 2010 Jan;77(1):92-6. doi: 10.1111/j.1399-0004.2009.01286.x. Epub 2009 Oct 5. Clin Genet. 2010. PMID: 19807736 No abstract available.
A teenager with a t(X;17)(q22;q25) and ovarian failure.
Martínez-Valenzuela M, Rivera H, Mundo-Ayala JN, González-Mercado MG, Davalos-Rodríguez IP. Martínez-Valenzuela M, et al. Among authors: mundo ayala jn. Genet Couns. 2010;21(3):269-75. Genet Couns. 2010. PMID: 20964116
Genetic analysis for carrier diagnosis in hemophilia A and B in the Mexican population: 25 years of experience.
González-Ramos IA, Mantilla-Capacho JM, Luna-Záizar H, Mundo-Ayala JN, Lara-Navarro IJ, Ornelas-Ricardo D, González Alcázar JÁ, Evangelista-Castro N, Jaloma-Cruz AR. González-Ramos IA, et al. Among authors: mundo ayala jn. Am J Med Genet C Semin Med Genet. 2020 Dec;184(4):939-954. doi: 10.1002/ajmg.c.31854. Epub 2020 Nov 15. Am J Med Genet C Semin Med Genet. 2020. PMID: 33191626