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Page 1
Donor splice-site mutations in WT1 are responsible for Frasier syndrome.
Barbaux S, Niaudet P, Gubler MC, Grünfeld JP, Jaubert F, Kuttenn F, Fékété CN, Souleyreau-Therville N, Thibaud E, Fellous M, McElreavey K. Barbaux S, et al. Among authors: souleyreau therville n. Nat Genet. 1997 Dec;17(4):467-70. doi: 10.1038/ng1297-467. Nat Genet. 1997. PMID: 9398852
[Genetic control of spermatogenesis: Y chromosome and male infertility].
Krausz C, Siffroi J, Souleyreau-Therville N, Bourgeron T, McElreavey K, Fellous M. Krausz C, et al. Among authors: souleyreau therville n. Ann Biol Clin (Paris). 1999 May;57(3):309-17. Ann Biol Clin (Paris). 1999. PMID: 10377481 Free article. Review. French. No abstract available.
A high frequency of Y chromosome deletions in males with nonidiopathic infertility.
Krausz C, Quintana-Murci L, Barbaux S, Siffroi JP, Rouba H, Delafontaine D, Souleyreau-Therville N, Arvis G, Antoine JM, Erdei E, Taar JP, Tar A, Jeandidier E, Plessis G, Bourgeron T, Dadoune JP, Fellous M, McElreavey K. Krausz C, et al. Among authors: souleyreau therville n. J Clin Endocrinol Metab. 1999 Oct;84(10):3606-12. doi: 10.1210/jcem.84.10.6040. J Clin Endocrinol Metab. 1999. PMID: 10523003