Publications by authors named "Marko Bertone"

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A mild phenotype of dihydropyrimidine dehydrogenase deficiency and developmental retardation associated with a missense mutation affecting cofactor binding.
Sabine Weidensee, Peter Goettig, Marko Bertone, Dorothea Haas, Viktor Magdolen

Clin Biochem· June 2011

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The genotype of the original Wiskott phenotype.
Vera Binder, Michael H Albert, Maria Kabus, Marko Bertone, Alfons Meindl

N Engl J Med· October 2006

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