The Presence of Clitoromegaly in the Nonclassical Form of 21-Hydroxylase Deficiency Could Be Partially Modulated by the CAG Polymorphic Tract of the Androgen Receptor Gene. [electronic resource]
Producer: 20160712Description: e0148548 p. digitalISSN:- 1932-6203
- 3-Oxo-5-alpha-Steroid 4-Dehydrogenase -- genetics
- Adolescent
- Adrenal Hyperplasia, Congenital -- diagnosis
- Adult
- Alleles
- Child
- Child, Preschool
- Clitoris -- pathology
- Female
- Gene Frequency
- Genetic Association Studies
- Genotype
- Humans
- Male
- Membrane Proteins -- genetics
- Mutation
- Phenotype
- Polymorphism, Genetic
- Receptors, Androgen -- genetics
- Severity of Illness Index
- Steroid 21-Hydroxylase -- blood
- Trinucleotide Repeat Expansion
- Trinucleotide Repeats
- X Chromosome Inactivation
- Young Adult
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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