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Dive into the research topics of 'Carriers of 21-hydroxylase deficiency are not at increased risk for hyperandrogenism'. Together they form a unique fingerprint.
Medicine & Life Sciences
Congenital adrenal hyperplasia due to 21 hydroxylase deficiency
Hyperandrogenism
Mutation
Androgens
Dehydroepiandrosterone Sulfate
Hyperplasia
Cosyntropin
17-alpha-Hydroxyprogesterone
Gene Conversion
Congenital Adrenal Hyperplasia
Hirsutism
Sex Hormone-Binding Globulin
Androstenedione
Population
Heterozygote
Menstrual Cycle
Parity
Inborn Genetic Diseases
Testosterone
Mothers
Weights and Measures
Confidence Intervals
Phenotype
Chemical Compounds
Steroid 21-Hydroxylase
Androgens
Dehydroepiandrosterone Sulfate
Adrenocorticotropic Hormone
Cosyntropin
17-alpha-Hydroxyprogesterone
Gene Conversion
Sex Hormone-Binding Globulin
Androstenedione
Level control
Testosterone
Defects