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	1.	[Waardenburg syndrome: neonatal diagnosis apropos of a case]. [electronic resource] by Nacher Fernández, A Vitoria Miñana, I Aguilera Olmos, R Buesa Ibáñez, E Producer: 19841121 In: Anales espanoles de pediatria vol. 20 Availability: No items available. Save to lists Add to cart (remove)
	2.	[Incontinentia pigmenti: neonatal diagnosis]. [electronic resource] by Aguilera Olmos, R Nacher Fernández, A Vitoria Miñana, I Mezquita Edo, C Labordena Barceló, C Buesa Ibáñez, E Producer: 19840214 In: Anales espanoles de pediatria vol. 19 Availability: No items available. Save to lists Add to cart (remove)
	3.	[Contiguous gene deletion syndrome in Xp21: the association between glycerol kinase deficiency, congenital suprarenal hypoplasia and Duchenne's muscular dystrophy]. [electronic resource] by Pantoja-Martínez, J Martínez-Castellano, F Tarazona-Casany, I Buesa-Ibáñez, E Ardid-Encinar, M Esparza-Sánchez, M A Bonet-Arzo, J Producer: 20071002 In: Revista de neurologia vol. 44 Availability: No items available. Save to lists Add to cart (remove)

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