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Detection of the heterozygous state in siblings of patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
Gutai, J P; Lee, P A; Johnsonbaugh, R E; Gareis, F; Urban, M D; Migeon, C J.
J Pediatr ; 94(5): 770-2, 1979 May.
Article in En | MEDLINE | ID: mdl-221633
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Collection: 01-internacional Database: MEDLINE Main subject: Steroid Hydroxylases / Adrenocortical Hyperfunction / Adrenal Hyperplasia, Congenital / Genetic Carrier Screening Type of study: Diagnostic_studies / Etiology_studies Limits: Humans Language: En Journal: J Pediatr Year: 1979 Document type: Article Country of publication: Estados Unidos
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Collection: 01-internacional Database: MEDLINE Main subject: Steroid Hydroxylases / Adrenocortical Hyperfunction / Adrenal Hyperplasia, Congenital / Genetic Carrier Screening Type of study: Diagnostic_studies / Etiology_studies Limits: Humans Language: En Journal: J Pediatr Year: 1979 Document type: Article Country of publication: Estados Unidos