Your search returned 2 results.

Results
	1.	Utility of phenylalanine hydroxylase genotype for tetrahydrobiopterin responsiveness classification in patients with phenylketonuria. [electronic resource] by Quirk, Meghan E Dobrowolski, Steven F Nelson, Benjamin E Coffee, Bradford Singh, Rani H Producer: 20130129 In: Molecular genetics and metabolism vol. 107 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Favism, the commonest form of severe hemolytic anemia in Palestinian children, varies in severity with three different variants of G6PD deficiency within the same community. [electronic resource] by Reading, N Scott Sirdah, Mahmoud M Shubair, Mohammad E Nelson, Benjamin E Al-Kahlout, Mustafa S Al-Tayeb, Jamal M Aboud, Lina N Shaban, Maysaa Abu Luzzatto, Lucio Prchal, Josef T Producer: 20180112 In: Blood cells, molecules & diseases vol. 60 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

Refine your search