HuGE Literature Finder
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| Identification of an SRY-negative 46,XX infertility male with a heterozygous deletion downstream of SOX3 gene. Molecular cytogenetics 2022 2 15 (1): 2. Qin Shengfang, Wang Xueyan, Wang J |
| Prevalence of Y chromosome microdeletion in azoospermia factor subregions among infertile men from West Bengal, India. Molecular genetics & genomic medicine 2021 Aug e1769. Dutta Saurav, Paladhi Pranab, Pal Samudra, Bose Gunja, Ghosh Papiya, Chattopadhyay Ratna, Chakravarty Baidyanath, Ghosh Suj |
| Variation analysis of SOX8 gene in Chinese men with non-obstructive azoospermia or oligozoospermia. Andrologia 2020 Feb e13531. Zhang Xu, Ning Yunna, Liu Wen, Zhang Taijian, Qin Yingying, Zhao Shidou, Cao Yongzhi, Zhang Hao |
| [Prenatal diagnosis for two fetuses carrying partial deletion of Y chromosome]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2020 2 37 (2): 182-185. Pang Hong, Gao Ming, Hua Jun, Tong Dan, Zhao Yanhui, Feng Xiaoji |
| Copy Number Variations of the Azoospermia Factor Region and SRY Are Not Associated with the Risk of Hypospadias. Sexual development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation 2016 10 (1): 12-5. Kon Masafumi, Saito Kazuki, Mitsui Takahiko, Miyado Mami, Igarashi Maki, Moriya Kimihiko, Nonomura Katsuya, Shinohara Nobuo, Ogata Tsutomu, Fukami Ma |
| Genetic Risk of Azoospermia Factor (AZF) Microdeletions in Idiopathic Cases of Azoospermia and Oligozoospermia in Central Indian Population. Journal of clinical and diagnostic research : JCDR 2014 Mar 8 (3): 88-91. Ambulkar Prafulla S, Sigh Ramji, Reddy Mvr, Varma Poonam S, Gupta Dilip O, Shende Moreshwar R, Pal Asoke |
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