Detection of the heterozygous state in siblings of patientswith congenital adrenal hyperplasia due to 21-hydroxylase deficiency

Authors :: Claude J. Migeon
Maria D. Urban
Roger E. Johnsonbaugh
James P. Gutai
Frank J. Gareis
Peter A. Lee
Source :: The Journal of Pediatrics. 94:770-772
Publication Year :: 1979
Publisher :: Elsevier BV, 1979.

Subjects :: medicine.medical_specialty
Adrenocortical Hyperfunction
Adrenal Hyperplasia, Congenital
business.industry
Genetic Carrier Screening
Homozygote
Adrenocorticotropic hormone
medicine.disease
Congenital adrenal hyperplasia due to 21-hydroxylase deficiency
Endocrinology
Adrenocorticotropic Hormone
Internal medicine
Steroid Hydroxylases
Pediatrics, Perinatology and Child Health
Hydroxyprogesterones
medicine
Humans
business
Progesterone

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