K. Sarafoglou

发表

Expanded newborn screening identifies maternal primary carnitine deficiency.

S. Cederbaum, N. Longo, M. Pasquali, 2007, Molecular genetics and metabolism.

High incidence of profound biotinidase deficiency detected in newborn screening blood spots in the Somalian population in Minnesota

D. Babovic‐Vuksanovic, D. Gavrilov, C. Anderson, 2009, Journal of Inherited Metabolic Disease.