HuGE Literature Finder
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Next-generation sequencing: toward an increase in the diagnostic yield in patients with apparently idiopathic spermatogenic failure. Asian journal of andrology 2020 Jul . Cannarella Rossella, Condorelli Rosita A, Paolacci Stefano, Barbagallo Federica, Guerri Giulia, Bertelli Matteo, La Vignera Sandro, Calogero Aldo |
Development of a novel next-generation sequencing panel for diagnosis of quantitative spermatogenic impairment. Journal of assisted reproduction and genetics 2020 4 37 (4): 753-762. Rocca Maria Santa, Msaki Aichi, Ghezzi Marco, Cosci Ilaria, Pilichou Kalliopi, Celeghin Rudy, Foresta Carlo, Ferlin Alber |
Human male infertility and its genetic causes. Reproductive medicine and biology 2017 12 16 (2): 81-88. Miyamoto Toshinobu, Minase Gaku, Shin Takeshi, Ueda Hiroto, Okada Hiroshi, Sengoku Kaz |
Validation and application of a novel integrated genetic screening method to a cohort of 1,112 men with idiopathic azoospermia or severe oligozoospermia. Human mutation 2017 8 38 (11): 1592-1605. Oud Manon S, Ramos Liliana, O'Bryan Moira K, McLachlan Robert I, Okutman Özlem, Viville Stephane, de Vries Petra F, Smeets Dominique F C M, Lugtenberg Dorien, Hehir-Kwa Jayne Y, Gilissen Christian, van de Vorst Maartje, Vissers Lisenka E L M, Hoischen Alexander, Meijerink Aukje M, Fleischer Kathrin, Veltman Joris A, Noordam Michiel |
Investigation of mutations in the synaptonemal complex protein 3 (SYCP3) gene among azoospermic infertile male patients in the Turkish population. Andrologia 2013 Apr 45 (2): 92-100. Gurkan H, Aydin F, Kad?oglu A, Palanduz |
Mutations of the SYCP3 gene in women with recurrent pregnancy loss. American journal of human genetics 2009 Jan 84 (1): 14-20. Bolor Hasbaira, Mori Terumi, Nishiyama Sachie, Ito Yoshimasa, Hosoba Eriko, Inagaki Hidehito, Kogo Hiroshi, Ohye Tamae, Tsutsumi Makiko, Kato Takema, Tong Maoqing, Nishizawa Haruki, Pryor-Koishi Kanako, Kitaoka Eri, Sawada Tomio, Nishiyama Yukio, Udagawa Yasuhiro, Kurahashi Hiro |
Mutations in the chromosome pairing gene FKBP6 are not a common cause of non-obstructive azoospermia. Molecular human reproduction 2005 Sep 11 (9): 673-5. Westerveld G H, Repping S, Lombardi M P, van der Veen |
Azoospermia in patients heterozygous for a mutation in SYCP3. Lancet (London, England) 2003 Nov 362 (9397): 1714-9. Miyamoto Toshinobu, Hasuike Shiga, Yogev Leah, Maduro Maria R, Ishikawa Mutsuo, Westphal Heiner, Lamb Dolores |
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