Search Results - Ibarra-Ramírez, Marisol

Clinical and genetic aspects of Turner’s syndrome by Ibarra Ramírez, Marisol, Martínez de Villarreal, Laura Elia

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Consulta genética y asesoramiento by Rodríguez Sánchez, Iram Pablo, Campos-Acevedo, Luis D., Ibarra-Ramírez, Marisol, López-Uriarte, Areli, Martínez-de-Villarreal, Laura E.

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Consulta génetica y asesoramiento by Rodríguez Sánchez, Irám Pablo, Campos Acevedo, Luis Daniel, Ibarra Ramírez, Marisol, López Uriarte, Areli, Martínez de Villarreal, Laura Elia

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Spondylothoracic dysostosis, Jarcho Levin syndrome: case report by Medina de la Cruz, Antonia Yesenia, Rodríguez Balderrama, Isaías, Burciaga Flores, Carlos Horacio, Martínez de Villarreal, Laura Elia, Ibarra Ramírez, Marisol, O Cavazos, Manuel Enrique de la

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Primary hypertrophic osteoarthropathy: report of two novel genetic variants in the SLCO2A1 gene in two Mexican patients by Ibarra Ramírez, Marisol, Villarreal Martínez, Alejandra, Vázquez Martínez, Osvaldo Tomás, Martínez de Villarreal, Laura Elia, Garay Mendoza, Domingo, Rodríguez Vivian, Candelario, Ocampo Candiani, Jorge, De La Rosa Marbán, Edgar

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Detection of Turner Syndrome by Quantitative PCR of SHOX and VAMP7 Genes by Ibarra Ramírez, Marisol, Zamudio Osuna, Michelle de Jesús, Campos Acevedo, Luis Daniel, Gallardo Blanco, Hugo Leonid, Cerda Flores, Ricardo Martín, Rodríguez Sánchez, Irám Pablo, Martínez de Villarreal, Laura Elia

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Gene Copy Number Quantification of SHOX , VAMP7 , and SRY for the Detection of Sex Chromosome Aneuploidies in Neonates by Ibarra Ramírez, Marisol, Lugo Trampe, José de Jesús, Campos Acevedo, Luis Daniel, Zamudio Osuna, Michelle de Jesús, Torres Muñoz, Iris Carmen, Gómez Puente, Viviana, García Castañeda, Gloria, Arredondo Vázquez, Patricia, Rodríguez Sánchez, Irám Pablo, Schaeffer, Satu Elisa, Velasco Sepúlveda, Braulio Hernán, Villarreal Pérez, Jesús Zacarías, Martínez de Villarreal, Laura Elia

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