Search Results - "CUNNIGHAM, R. D"

Carriers of 21-hydroxylase deficiency are not at increased risk for hyperandrogenism by KNOCHENHAUER, E. S, CORTET-RUDELLI, C, CUNNIGHAM, R. D, CONWAY-MYERS, B. A, DEWAILLY, D, AZZIZ, R

“…A deficiency of 21-hydroxylase activity is one of the most commonly inherited genetic disorders in man, with heterozygosity for CYP21 mutations affecting…”
Get full text

Carriers of 21-Hydroxylase Deficiency Are Not at Increased Risk for Hyperandrogenism1 by Knochenhauer, E. S, Cortet-Rudelli, C, Cunnigham, R. D, Conway-Myers, B. A, Dewailly, D, Azziz, R

“…A deficiency of 21-hydroxylase activity is one of the most commonly inherited genetic disorders in man, with heterozygosity for CYP21 mutations affecting…”
Get full text

Carriers of 21-Hydroxylase Deficiency Are Not at Increased Risk for Hyperandrogenism by Knochenhauer, E. S., Cortet-Rudelli, C., Cunnigham, R. D., Conway-Myers, B. A., Dewailly, D., Azziz, R.

“…Abstract A deficiency of 21-hydroxylase activity is one of the most commonly inherited genetic disorders in man, with heterozygosity for CYP21 mutations…”
Get full text