Clinical Studies in Medical Biochemistry

Clinical Studies in Medical Biochemistry

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The fragile X mutation involves expression of a CGG repeat stretch in the 5a#39; encoding region of FMR1. ... were diagnosed as having fragile X syndrome, and the mother, sister, uncle, and maternal grandmother as fragile X premutation carriers.

Title:Clinical Studies in Medical Biochemistry
Author: Department of Biochemistry University of New Mexico Robert H. Glew Professor and Chairman, Miriam D. Rosenthal Professor of Biochemistry Eastern Virginia Medical School
Publisher:Oxford University Press, USA - 2006-08-07

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