Pages that link to "Q74088241"

The following pages link to Hyperandrogenism and Manifesting Heterozygotes for 21-Hydroxylase Deficiency (Q74088241):

Displaying 19 items.

• The presence of the 21-hydroxylase deficiency carrier status in hirsute women: phenotype-genotype correlations (Q28374323) (← links)
• Congenital adrenal hyperplasia: epidemiology, management and practical drug treatment (Q34385493) (← links)
• Genetic approaches to stature, pubertal timing, and other complex traits (Q35563817) (← links)
• The Genetic Basis of the Polycystic Ovary Syndrome: A Literature Review Including Discussion of PPAR-gamma. (Q35676497) (← links)
• The adrenal and polycystic ovary syndrome (Q36969178) (← links)
• The Pathogenesis of Polycystic Ovary Syndrome (PCOS): The Hypothesis of PCOS as Functional Ovarian Hyperandrogenism Revisited (Q41640666) (← links)
• Clinical manifestations and hormonal profile of two women with Cushing's disease and mild deficiency of 21-hydroxylase (Q45271019) (← links)
• Characterization of novel missense mutations in CYP21 causing congenital adrenal hyperplasia. (Q48083334) (← links)
• Children with premature pubarche: is an alterated neonatal 17-Ohp screening test a predictive factor? (Q50024650) (← links)
• A variant of the glucocorticoid receptor gene is not associated with adrenal androgen excess in women with polycystic ovary syndrome (Q59549324) (← links)
• No association between body mass index and beta(3)-adrenergic receptor variant (W64R) in children with premature pubarche and adolescent girls with hyperandrogenism (Q73479919) (← links)
• Human chorionic gonadotropin stimulation to assess for ovarian hyperandrogenism (Q74567177) (← links)
• Structural and functional analysis of a novel mutation of CYP21B in a heterozygote carrier of 21-hydroxylase deficiency (Q80390530) (← links)
• Polycystic ovary syndrome in adolescence (Q81017308) (← links)
• Genetics of polycystic ovary syndrome (Q82245844) (← links)
• Hyperandrogenism in carriers of CYP21 mutations: the role of genotype (Q83377310) (← links)
• Genotype in the diagnosis of 21-hydroxylase deficiency: who should undergo CYP21A2 analysis? (Q86068364) (← links)
• The prevalence of heterozygous CYP21A2 deficiency in patients with idiopathic acne, hirsutism, or both (Q90665525) (← links)
• Genotype-phenotype correlations in children and adolescents with nonclassical congenital adrenal hyperplasia due to 21-hydroxylase deficiency (Q97546875) (← links)