Human Genome Epidemiology Literature Finder
Records 1 - 11 (of 11 Records) |
Query Trace: NR0B1[original query] |
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Uniparental Disomy in Somatic Mosaicism 45,X/46,XY/46,XX Associated with Ambiguous Genitalia. Sexual development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation 2015 9 (3): 136-43. Serra Alexandre, Denzer Friederike, Hiort Olaf, Barth Thomas F, Henne-Bruns Doris, Barbi Gotthold, Rettenberger Günther, Wabitsch Martin, Just Walter, Leriche Clothil |
Hormone-related pathways and risk of breast cancer subtypes in African American women. Breast cancer research and treatment 2015 Oct . Haddad Stephen A, Lunetta Kathryn L, Ruiz-Narváez Edward A, Bensen Jeannette T, Hong Chi-Chen, Sucheston-Campbell Lara E, Yao Song, Bandera Elisa V, Rosenberg Lynn, Haiman Christopher A, Troester Melissa A, Ambrosone Christine B, Palmer Julie |
Genetic Screening of Iranian Patients with 46,XY Disorders of Sex Development. Reports of biochemistry & molecular biology 2017 11 6 (1): 59-65. Shojaei Azadeh, Ebrahimzadeh-Vesal Reza, Ahani Ali, Razzaghy-Azar Maryam, Khakpour Golnaz, Ghazi Farideh, Tavakkoly-Bazzaz Jav |
[Genetic analysis of a 46,XY female with sex reversal due to duplication of NR0B1 gene]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2018 12 35 (6): 804-807. Qin Shengfang, Wang Xueyan, Li Yunxi |
De novo mutations in idiopathic male infertility-A pilot study. Andrology 2020 8 9 (1): 212-220. Hodži? Alenka, Maver Aleš, Plaseska-Karanfilska Dijana, Ristanovi? Mom?ilo, Noveski Predrag, Zorn Branko, Terzic Marija, Kunej Tanja, Peterlin Bor |
Screening for structural variants of four candidate genes in dogs with disorders of sex development revealed the first case of a large deletion in NR5A1. Animal reproduction science 2020 10 223 106632. Nowacka-Woszuk Joanna, Szczerbal Izabela, Stachowiak Monika, Dzimira Stanislaw, Nizanski Wojciech, Biezynski Janusz, Nowak Tomasz, Gogulski Maciej, Switonski Mar |
Development and Verification of the Hypoxia- and Immune-Associated Prognostic Signature for Pancreatic Ductal Adenocarcinoma. Frontiers in immunology 2021 10 12 728062. Chen Dongjie, Huang Hui, Zang Longjun, Gao Wenzhe, Zhu Hongwei, Yu Xi |
Genomic testing for copy number and single nucleotide variants in spermatogenic failure. Journal of assisted reproduction and genetics 2022 Jul . Hardy J, Pollock N, Gingrich T, Sweet P, Ramesh A, Kuong J, Basar A, Jiang H, Hwang K, Vukina J, Jaffe T, Olszewska M, Kurpisz M, Yatsenko A |
WT1, NR0B1, NR5A1, LHX9, ZFP92, ZNF275, INSL3, and NRIP1 Genetic Variants in Patients with Premature Ovarian Insufficiency in a Mexican Cohort. Genes 2022 4 13 (4): . Ramos Lu |
Role of chromosomal imbalances in the pathogenesis of DSD: A retrospective analysis of 115 prenatal samples. European journal of medical genetics 2023 3 66 (6): 104748. Mary L, Fradin M, Pasquier L, Quelin C, Loget P, Le Lous M, Le Bouar G, Nivot-Adamiak S, Lokchine A, Dubourg C, Jauffret V, Nouyou B, Henry C, Launay E, Odent S, Jaillard S, Belaud-Rotureau M |
Phenotype and genetic characteristics in 20 Chinese patients with 46,XY disorders of sex development. Journal of endocrinological investigation 2023 2 . Zheng G Y, Chu G M, Li P P, He |
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- Page last updated:Apr 22, 2024
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