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Trotter, D
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1
EVIDENCE FOR INDEPENDENT MUTATION OF THE 21-HYDROXYLASE DEFICIENCY (210H DEF) GENE IN ALASKAN ESKIMOS WITH CONGENITAL ADRENAL HYPERPLASIA (CAH)
by
Petersen, G M
,
MacCracken, J E
,
Rotter, J I
,
Trotter
,
D
,
New, M I
,
Park, M S
,
Terasaki, P I
,
Sparkes, R S
,
Ward, J I
Published in
Pediatric Research
(1984)
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Pediatrics, Perinatology, and Child Health
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