专题:Sexual Differentiation and Disorders

This cluster of papers explores the molecular biology, biochemistry, and physiology of human steroidogenesis, focusing on disorders such as Congenital Adrenal Hyperplasia and Intersex Disorders. It delves into topics like androgen receptor gene mutations, prenatal hormone effects on sexual differentiation, digit ratio as a marker for prenatal hormone action, and the influence of fetal testosterone on gender identity and behavior.
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Survival without treatment of patients with classic and nonclassic 21-hydroxylase deficiency: a multicenter retrospective cohort study

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Clinical practice guidelines "Congenital adrenal hyperplasia in children" with comments

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Genotype-refined 17OHP cut-offs diagnosing nonclassical CAH due to 21OH deficiency in children with premature pubarche

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Clinical Presentation and Early Outcomes of Congenital Endocrine Salt‐Wasting Syndromes Unrelated to 21‐Hydroxylase Deficiency

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Validation of DSD Interpreter, a Mobile Application for Point-of-Care Evaluation of Infants with Atypical Genitalia: Correspondence

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Machine learning algorithms to accelerate etiological diagnosis of congenital disorders of adrenal steroidogenesis

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Adrenal insufficiency after long-term high-dose ethinylestradiol use in a transgender woman

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Codierung und Decodierung sexueller Entwicklung

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Navigating the Semantic Labyrinth of “Sex” in the Study of Reproductive Trait Evolution

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Clinical and endocrine correlates of genetic etiologies in severe hypospadias: Study from 34 patients

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