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	1.	A del(13)(q21.32q31.2)dn refined to 21.9 Mb in a female toddler with irides heterochromia and hypopigmentation: appraisal of interstitial mid-13q deletions. [electronic resource] by Córdova-Fletes, Carlos Rivera, Horacio Garza-Villarreal, Eduardo A Vázquéz-Cárdenas, Norma A Martínez-Jacobo, Lizeth A Moreno-Andrade, Talia Producer: 20170206 In: Clinical dysmorphology vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	[Genotype-phenotype discordance in a Duchenne muscular dystrophy patient due to a novel mutation: insights into the shock absorber function of dystrophin]. [electronic resource] by López-Hernández, Luz B van Heusden, Dave Soriano-Ursúa, Marvin A Figuera-Villanueva, Luis Vázquez-Cárdenas, Norma A Canto, Patricia Gómez-Díaz, Benjamín Coral-Vázquez, Ramón M Producer: 20110829 In: Revista de neurologia vol. 52 Availability: No items available. Save to lists Add to cart (remove)
	3.	[Diagnosis and treatment with steroids for patients with Duchenne muscular dystrophy: experience and recommendations for Mexico. Administración del Patrimonio de la Beneficencia Pública. Asociación de Distrofia Muscular de Occidente]. [electronic resource] by Vázquez-Cárdenas, Norma A Ibarra-Hernández, Francisco López-Hernández, Luz B Escobar-Cedillo, Rosa E Ruano-Calderón, Luis A Gómez-Díaz, Benjamín García-Calderón, Noemí Carriedo-Dávila, M Fernanda Rojas-Hurtado, Liliana G Luna-Padrón, Emilia Coral-Vázquez, Ramón M Producer: 20140624 In: Revista de neurologia vol. 57 Availability: No items available. Save to lists Add to cart (remove)