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Associations between restriction fragment length polymorphisms detected with a probe for human 21-hydroxylase (21-OH) and two clinical forms of 21-OH deficiency

21-Oh DeficiencyMendelian DisorderClinical FormsGenetic DisorderGeneticsInherited Metabolic DiseaseHuman PolymorphismPathologyMolecular GeneticsMedical GeneticsMedicineClinical Genetics