Human Genome Epidemiology Literature Finder
Records 1 - 7 (of 7 Records) |
Query Trace: Hirsutism and CYP21A2[original query] |
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Clinical and molecular characterization of a cohort of 161 unrelated women with nonclassical congenital adrenal hyperplasia due to 21-hydroxylase deficiency and 330 family members. The Journal of clinical endocrinology and metabolism 2009 May 94 (5): 1570-8. Bidet Maud, Bellanné-Chantelot Christine, Galand-Portier Marie-Béatrice, Tardy Véronique, Billaud Line, Laborde Kathleen, Coussieu Christiane, Morel Yves, Vaury Christelle, Golmard Jean-Louis, Claustre Aurélie, Mornet Etienne, Chakhtoura Zeina, Mowszowicz Irene, Bachelot Anne, Touraine Philippe, Kuttenn Frédériq |
Fertility in women with nonclassical congenital adrenal hyperplasia due to 21-hydroxylase deficiency. The Journal of clinical endocrinology and metabolism 2010 1 95 (3): 1182-90. Bidet Maud, Bellanné-Chantelot Christine, Galand-Portier Marie-Béatrice, Golmard Jean-Louis, Tardy Véronique, Morel Yves, Clauin Séverine, Coussieu Christiane, Boudou Philippe, Mowzowicz Irene, Bachelot Anne, Touraine Philippe, Kuttenn |
CYP21A2 genotypes do not predict the severity of hyperandrogenic manifestations in the nonclassical form of congenital adrenal hyperplasia. Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et métabolisme 2013 Apr 45 (4): 301-7. Moura-Massari V O, Bugano D D G, Marcondes J A M, Gomes L G, Mendonca B B, Bachega T A S |
Comprehensive genotyping of Turkish women with hirsutism. Journal of endocrinological investigation 2019 2 42 (9): 1077-1087. Polat S, Karaburgu S, Ünlühizarc? K, Dündar M, Özkul Y, Arslan Y K, Karaca Z, Kelestimur |
Clinical and hormonal characteristics in heterozygote carriers of congenital adrenal hyperplasia. The Journal of steroid biochemistry and molecular biology 2019 Dec 105554. Guarnotta Valentina, Niceta Marcello, Bono Marianna, Marchese Serena, Fabiano Carmelo, Indelicato Serena, Di Gaudio Francesca, Garofalo Piernicola, Giordano Car |
The prevalence of heterozygous CYP21A2 deficiency in patients with idiopathic acne, hirsutism, or both. Endocrine 2019 Oct . Gao Yinjie, Yu Bingqing, Mao Jiangfeng, Wang Xi, Nie Min, Wu Xuey |
Non-Classical Congenital Adrenal Hyperplasia-Causing Alleles in Adolescent Girls with PCOS and in Risk Group for PCOS Development. Diagnostics (Basel, Switzerland) 2021 6 11 (6): . Lidaka Lasma, Bekere Laine, Lazdane Gunta, Dzivite-Krisane Iveta, Kivite-Urtane Anda, Gailite Lin |
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- Page last updated:Mar 25, 2024
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