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Wilson, Robert
One or more keywords matched the following items that are connected to
Wilson, Robert
Item Type
Name
Academic Article
A genetic defect resulting in mild low-renin hypertension.
Academic Article
Intrauterine growth retardation associated with maternal uniparental disomy for chromosome 6 unmasked by congenital adrenal hyperplasia.
Academic Article
Prevalence of mild apparent mineralocorticoid excess in Mennonites.
Academic Article
Prenatal diagnosis for congenital adrenal hyperplasia in 532 pregnancies.
Academic Article
In vitro expression studies of a novel mutation delta299 in a patient affected with apparent mineralocorticoid excess.
Concept
Homozygote
Search Criteria
Homozygote