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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
Steroid disorders in children: congenital adrenal hyperplasia and apparent mineralocorticoid excess.
Academic Article
Resistance to multiple steroids in two sisters.
Academic Article
Prenatal diagnosis and treatment of 11beta-hydroxylase deficiency congenital adrenal hyperplasia resulting in normal female genitalia.
Academic Article
Intrauterine growth retardation associated with maternal uniparental disomy for chromosome 6 unmasked by congenital adrenal hyperplasia.
Academic Article
Resistance to several steroids in two sisters.
Academic Article
Prevalence of mild apparent mineralocorticoid excess in Mennonites.
Academic Article
Apparent mineralocorticoid excess.
Academic Article
In vitro expression studies of a novel mutation delta299 in a patient affected with apparent mineralocorticoid excess.
Academic Article
Update on the prenatal diagnosis and treatment of congenital adrenal hyperplasia due to 11beta-hydroxylase deficiency.
Concept
Pedigree
Academic Article
Molecular genetic analysis in 93 patients and 193 family members with classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency in Croatia.
Search Criteria
Pedigree