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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. Genet Couns. 2010;21(3):269-75. Genet Couns. 2010. PMID: 20964116
Williams-Beuren syndrome in Mexican patients confirmed by FISH and assessed by aCGH.
Ramírez-Velazco A, Aguayo-Orozco TA, Figuera L, Rivera H, Jave-Suárez L, Aguilar-Lemarroy A, Torres-Reyes LA, Córdova-Fletes C, Barros-Núñez P, Delgadillo-Pérez S, Dávalos-Rodríguez IP, García-Ortiz JE, Domínguez MG. Ramírez-Velazco A, et al. Among authors: davalos rodriguez ip. J Genet. 2019 Jun;98(2):34. J Genet. 2019. PMID: 31204697 Free article.
[New subtype of familial achondrogenesis type IA (Houston-Harris)].
Ramírez-García SA, García-Cruz D, Cervantes-Aragón I, Bitar-Alatorre WE, Dávalos-Rodríguez IP, Dávalos-Rodríguez NO, Corona-Rivera JR, Sánchez-Corona J. Ramírez-García SA, et al. Cir Cir. 2018;86(1):89-98. doi: 10.24875/CIRU.M18000008. Cir Cir. 2018. PMID: 29681641 Spanish.
[Non-syndromic cleft lip/cleft palate and C677T methylene-tetrahydrofolate reductase variant in Mexican children].
Dávalos-Rodríguez IP, Ramírez-Lizardo EJ, Mena JP, Ledezma-Rodríguez V, Omayra-Dávalos N, González-Mercado MG, Durán-González J, Morán-Moguel MC, Peralta-Leal V, Salazar-Páramo M, Ledezma-Gómez V. Dávalos-Rodríguez IP, et al. Rev Med Inst Mex Seguro Soc. 2009 Sep-Oct;47(5):549-52. Rev Med Inst Mex Seguro Soc. 2009. PMID: 20550866 Spanish.
The association between the 844ins68 polymorphism in the CBS gene and breast cancer.
Gallegos-Arreola MP, Figuera-Villanueva LE, Ramos-Silva A, Salas-González E, Puebla-Pérez AM, Peralta-Leal V, García-Ortiz JE, Dávalos-Rodríguez IP, Zúñiga-González GM. Gallegos-Arreola MP, et al. Arch Med Sci. 2014 Dec 22;10(6):1214-24. doi: 10.5114/aoms.2014.47830. Arch Med Sci. 2014. PMID: 25624861 Free PMC article.
37 results