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208 results

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FOXO3a variants in patients with premature ovarian failure.
Vinci G, Christin-Maitre S, Pasquier M, Bouchard P, Fellous M, Veitia RA. Vinci G, et al. Among authors: veitia ra. Clin Endocrinol (Oxf). 2008 Mar;68(3):495-7. doi: 10.1111/j.1365-2265.2007.03052.x. Epub 2007 Sep 19. Clin Endocrinol (Oxf). 2008. PMID: 17888023 No abstract available.
BMP15 and premature ovarian failure: causal mutations, variants, polymorphisms?
Lakhal B, Laissue P, Braham R, Elghezal H, Saâd A, Fellous M, Veitia RA. Lakhal B, et al. Among authors: veitia ra. Clin Endocrinol (Oxf). 2010 Mar;72(3):425-6. doi: 10.1111/j.1365-2265.2009.03651.x. Epub 2009 Jun 8. Clin Endocrinol (Oxf). 2010. PMID: 19508678 No abstract available.
Mutations and sequence variants in GDF9 and BMP15 in patients with premature ovarian failure.
Laissue P, Christin-Maitre S, Touraine P, Kuttenn F, Ritvos O, Aittomaki K, Bourcigaux N, Jacquesson L, Bouchard P, Frydman R, Dewailly D, Reyss AC, Jeffery L, Bachelot A, Massin N, Fellous M, Veitia RA. Laissue P, et al. Among authors: veitia ra. Eur J Endocrinol. 2006 May;154(5):739-44. doi: 10.1530/eje.1.02135. Eur J Endocrinol. 2006. PMID: 16645022
Genome-wide linkage in a highly consanguineous pedigree reveals two novel loci on chromosome 7 for non-syndromic familial Premature Ovarian Failure.
Caburet S, Zavadakova P, Ben-Neriah Z, Bouhali K, Dipietromaria A, Charon C, Besse C, Laissue P, Chalifa-Caspi V, Christin-Maitre S, Vaiman D, Levi G, Veitia RA, Fellous M. Caburet S, et al. Among authors: veitia ra. PLoS One. 2012;7(3):e33412. doi: 10.1371/journal.pone.0033412. Epub 2012 Mar 13. PLoS One. 2012. PMID: 22428046 Free PMC article.
The X chromosome and ovarian function.
Vialard F, Cocquet J, Christin-Maitre S, Veitia R, Fellous M. Vialard F, et al. Cytogenet Genome Res. 2002;99(1-4):218-23. doi: 10.1159/000071596. Cytogenet Genome Res. 2002. PMID: 12900567 Review. No abstract available.
208 results