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A novel follicle-stimulating hormone receptor mutation causing primary ovarian failure: a fertility application of whole exome sequencing Bramble, Matthew S.; Goldstein, Ellen H.; Lipson, Allen; Ngun, Tuck; Eskin, Ascia; Gosschalk, Jason E.; Roach, Lara; Vashist, Neerja; Barseghyan, Hayk; Lee, Eric; Arboleda, Valerie A.; Vaiman, Daniel; Yuksel, Zafer; Fellous, Marc; Vilain, Eric 分享 收藏
Genome Editing and Dialogic Responsibility: What's in a Name? Blasimme, Alessandro; Anegon, Ignacio; Concordet, Jean-Paul; De Vos, John; Dubart-Kupperschmitt, Anne; Fellous, Marc; Fouchet, Pierre; Frydman, Nelly; Giovannangeli, Carine; Jouannet, Pierre; Serre, Jean-Loius; Steffann, Julie; Rial-Sebbag, Emmanuelle; Thomsen, Mogens; Cambon-Thomsen, Anne 分享 收藏
Mutant Cohesin in Premature Ovarian Failure Caburet, Sandrine; Arboleda, Valerie A.; Llano, Elena; Overbeek, Paul A.; Luis Barbero, Jose; Oka, Kazuhiro; Harrison, Wilbur; Vaiman, Daniel; Ben-Neriah, Ziva; Garcia-Tunon, Ignacio; Fellous, Marc; Pendas, Alberto M.; Veitia, Reiner A.; Vilain, Eric 分享 收藏
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CITED2 mutations potentially cause idiopathic premature ovarian failure Janeth Fonseca, Dora; Ojeda, Diego; Lakhal, Besma; Braham, Rim; Eggers, Stefanie; Turbitt, Erin; White, Stefan; Grover, Sonia; Warne, Garry; Zacharin, Margaret; Nevin Lam, Alexandra; Landolsi, Hanene; Elghezal, Hatem; Saad, Ali; Martin Restrepo, Carlos; Fellous, Marc; Sinclair, Andrew; Koopman, Peter; Laissue, Paul 分享 收藏
North African Jewish and non-Jewish populations form distinctive, orthogonal clusters Campbell, Christopher L.; Palamara, Pier F.; Dubrovsky, Maya; Botigue, Laura R.; Fellous, Marc; Atzmon, Gil; Oddoux, Carole; Pearlman, Alexander; Hao, Li; Henn, Brenna M.; Burns, Edward; Bustamante, Carlos D.; Comas, David; Friedman, Eitan; Pe'er, Itsik; Ostrer, Harry 分享 收藏
Genetic male infertility and mutation of CATSPER ion channels Hildebrand, Michael S.; Avenarius, Matthew R.; Fellous, Marc; Zhang, Yuzhou; Meyer, Nicole C.; Auer, Jana; Serres, Catherine; Kahrizi, Kimia; Najmabadi, Hossein; Beckmann, Jacques S.; Smith, Richard J. H. 分享 收藏
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Functional evidence implicating FOXL2 in non-syndromic premature ovarian failure and in the regulation of the transcription factor OSR2 Laissue, P.; Lakhal, B.; Benayoun, B. A.; Dipietromaria, A.; Braham, R.; Elghezal, H.; Philibert, P.; Saad, A.; Sultan, C.; Fellous, M.; Veitia, R. A. 分享 收藏
Identification of 34 Novel and 56 Known FOXL2 Mutations in Patients With Blepharophimosis Syndrome 在患有睑裂综合征的患者中鉴定34种新的和56种已知的FOXL2突变 Beysen, Diane; De Jaegere, Sarah; Amor, David; Bouchard, Philippe; Christin-Maitre, Sophie; Fellous, Marc; Touraine, Philippe; Grix, Arthur W.; Hennekam, Raoul; Meire, Francoise; Oyen, Nina; Wilson, Louise C.; Barel, Dalit; Clayton-Smith, Jill; de Ravel, Thomy; Decock, Christian; Delbeke, Patricia; Ensenauer, Regina; Ebinger, Friedrich; Gillessen-Kaesbach, Gabriele; Hendriks, Yvonne; Kimonis, Virginia; Laframboise, Rachel; Laissue, Paul; Leppig, Kathleen; Leroy, Bart P.; Miller, David T.; Mowat, David; Neumann, Luitgard; Plomp, Astrid; Van Regemorter, Nicole; Wieczorek, Dagmar; Veitia, Reiner A.; De Paepe, Anne; De Baere, Elfride 分享 收藏
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FOXL2 and SOX9 as parameters of female and male gonadal differentiation in patients with various forms of disorders of sex development (DSD) Hersmus, R.; Kalfa, N.; de Leeuw, B.; Stoop, H.; Oosterhuis, J. W.; de Krijger, R.; Wolffenbuttel, K. P.; Drop, S. L. S.; Veitia, R. A.; Fellous, M.; Jaubert, F.; Looijenga, L. H. J. 分享 收藏
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