Human Genome Epidemiology Literature Finder
Records 1 - 5 (of 5 Records) |
Query Trace: Amenorrhea and NR5A1[original query] |
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Limited contribution of NR5A1 (SF-1) mutations in women with primary ovarian insufficiency (POI). Fertility and sterility 2012 Jan 97 (1): 141-6.e2. Janse Femi, de With Larissa M, Duran Karen J, Kloosterman Wigard P, Goverde Angelique J, Lambalk Cornelius B, Laven Joop S E, Fauser Bart C J M, Giltay Jacques C, |
NR5A1 (SF-1) mutations are not a major cause of primary ovarian insufficiency. The Journal of clinical endocrinology and metabolism 2013 May 98 (5): E1017-21. Voican Adela, Bachelot Anne, Bouligand Jérôme, Francou Bruno, Dulon Jérôme, Lombès Marc, Touraine Philippe, Guiochon-Mantel An |
Novel Heterozygous Mutations of NR5A1 and Their Functional Characteristics in Patients with 46,XY Disorders of Sex Development without Adrenal Insufficiency. Hormone research in pædiatrics 2015 84 (2): 116-23. Woo Kyu Ha, Cheon Buwon, Kim Ja Hye, Cho Jahyang, Kim Gu-Hwan, Yoo Han-Wook, Choi Jin- |
Molecular study and genotype-phenotype in Chinese female patients with 46, XY disorders of sex development. Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology 2021 8 37 (10): 934-940. Xia Junke, Wu Jing, Chen Chen, Zhao Zhenhua, Xie Yanchuan, Bai Zhouxian, Kong Xiangdo |
Next Generation Sequencing Should Be Proposed to Every Woman With "Idiopathic" Primary Ovarian Insufficiency. Journal of the Endocrine Society 2021 6 5 (7): bvab032. Eskenazi Sarah, Bachelot Anne, Hugon-Rodin Justine, Plu-Bureau Genevieve, Gompel Anne, Catteau-Jonard Sophie, Molina-Gomes Denise, Dewailly Didier, Dodé Catherine, Christin-Maitre Sophie, Touraine Philip |
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