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Wolff, Daynna

One or more keywords matched the following items that are connected to Wolff, Daynna

Item Type	Name
Academic Article	Clinical, genetic, and biophysical characterization of a homozygous HERG mutation causing severe neonatal long QT syndrome.
Academic Article	Detection of an apparent homozygous 3120G>A cystic fibrosis mutation on a routine carrier screen.
Concept	Homozygote
Academic Article	First Report of Prenatal Ascertainment of a Fetus With Homozygous Loss of the SOX10 Gene and Phenotypic Correlation by Autopsy Examination.

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