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	1.	Phenylalanine hydroxylase deficiency in Mexico: genotype-phenotype correlations, BH4 responsiveness and evidence of a founder effect. [electronic resource] by Vela-Amieva, M Abreu-González, M González-del Angel, A Ibarra-González, I Fernández-Lainez, C Barrientos-Ríos, R Monroy-Santoyo, S Guillén-López, S Alcántara-Ortigoza, M A Producer: 20160302 In: Clinical genetics vol. 88 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Clinical, Cytogenetic, and Biochemical Analyses of a Family with a t(3;13)(q26.2;p11.2): Further Delineation of 3q Duplication Syndrome. [electronic resource] by Abreu-González, M García-Delgado, C Cervantes, A Aparicio-Onofre, A Guevara-Yáñez, R Sánchez-Urbina, R Gallegos-Arreola, M P Luna-Angulo, A Estrada, F J Morán-Barroso, V F Producer: 20131023 In: Case reports in genetics vol. 2013 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Clinical delineation of a patient with trisomy 1q32.qter and monosomy 5p resulting from a familial translocation 1;5. [electronic resource] by Flores Ramírez, F Abreu González, M García Delgado, C Aparicio Onofre, A Guevara Yáñez, R Sánchez Urbina, R Murguía Peniche, T Ramírez-Ortíz, M A Ibarra Ríos, D Ortiz de Luna, R I Cervantes Peredo, A B Morán Barroso, V F Producer: 20110302 In: Genetic counseling (Geneva, Switzerland) vol. 21 Availability: No items available. Save to lists Add to cart (remove)