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	1.	Determination of SCN1A genetic variants in Mexican patients with refractory epilepsy and Dravet syndrome. [electronic resource] by Jiménez-Arredondo, R E Brambila-Tapia, A J L Mercado-Silva, F M Magaña-Torres, M T Figuera, L E Producer: 20170928 In: Genetics and molecular research : GMR vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	SEVERE HYDROCEPHALUS, KIDNEY AND SKELETAL ANOMALIES IN A FEMALE PATIENT WITH MILD NEUROLOGICAL ALTERATIONS. [electronic resource] by Brambila-Tapia, A J L Wegman-Ostrosky, T Garcia-Cruz, D Figuera, L E Castañeda-Cisneros, G Jimenez-Arredondo, R E Sanchez-Corona, J Garcia-Ortiz, J E Producer: 20181016 In: Genetic counseling (Geneva, Switzerland) vol. 27 Availability: No items available. Save to lists Add to cart (remove)
	3.	Pure 9p trisomy derived from a terminal balanced unreciprocal translocation. [electronic resource] by Brambila-Tapia, A J L Neira, V A Vásquez-Velásquez, A I Jimenez-Arredondo, R E Chávez-González, E L Picos-Cárdenas, V J Fletes-Rayas, A L Figuera, L E Producer: 20141211 In: Genetic counseling (Geneva, Switzerland) vol. 25 Availability: No items available. Save to lists Add to cart (remove)

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