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Original Article

The Incidence of 21α-Hydroxylase Deficiency in Greek Hyperandrogenic Women: Screening and Diagnosis

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Pages 89-96 | Published online: 07 Jul 2009

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Eftihios Trakakis, George Basios, Pantelis Trompoukis, George Labos, Ioannis Grammatikakis & Demetrios Kassanos. (2010) An update to 21-hydroxylase deficient congenital adrenal hyperplasia. Gynecological Endocrinology 26:1, pages 63-71.
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Articles from other publishers (5)

E. Trakakis, E. Papadavid, M. Dalamaga, D Koumaki, N. Stavrianeas, D. Rigopoulos, G. Creatsas & D. Kassanos. (2013) Prevalence of non classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency in Greek women with acne: a hospital-based cross-sectional study. Journal of the European Academy of Dermatology and Venereology 27:11, pages 1448-1451.
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A. P. Barannik, A. A. Koltunova, L. A. Ozolinya, N. V. Lavrova, I. A. Shilov, I. I. Guzov & L. I. Patrushev. (2010) A new DNA diagnostic system for the detection of human CYP21 gene mutations associated with adrenal cortex hyperplasia. Russian Journal of Bioorganic Chemistry 36:3, pages 325-335.
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Eftihios Trakakis, Constantine Loghis & Demetrios Kassanos. (2009) Congenital Adrenal Hyperplasia Because of 21-Hydroxylase Deficiency. Obstetrical & Gynecological Survey 64:3, pages 177-189.
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Eftihios TRAKAKIS, Demetrios RIZOS, Constantine LOGHIS, Athanassios CHRYSSIKOPOULOS, Marilyn SPYROPOULOU, Emannuel SALAMALEKIS, George SIMEONIDES, Vassilis VAGOPOULOS, George SALAMALEKIS & Demetrios KASSANOS. (2008) The Prevalence of Non-classical Congenital Adrenal Hyperplasia Due to 21-hydroxylase Deficiency in Greek Women with Hirsutism and Polycystic Ovary Syndrome. Endocrine Journal 55:1, pages 33-39.
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E. Trakakis, D. Laggas, E. Salamalekis & G. Creatsas. (2014) 21-hydroxylase deficiency: From molecular genetics to clinical presentation. Journal of Endocrinological Investigation 28:4, pages 187-192.
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