HuGE Literature Finder
Records 1 - 6
| 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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