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SEMA3A deletion in a family with Kallmann syndrome validates the role of semaphorin 3A in human puberty and olfactory system development.
Young J, Metay C, Bouligand J, Tou B, Francou B, Maione L, Tosca L, Sarfati J, Brioude F, Esteva B, Briand-Suleau A, Brisset S, Goossens M, Tachdjian G, Guiochon-Mantel A. Young J, et al. Among authors: bouligand j. Hum Reprod. 2012 May;27(5):1460-5. doi: 10.1093/humrep/des022. Epub 2012 Mar 12. Hum Reprod. 2012. PMID: 22416012
Isolated familial hypogonadotropic hypogonadism and a GNRH1 mutation.
Bouligand J, Ghervan C, Tello JA, Brailly-Tabard S, Salenave S, Chanson P, Lombès M, Millar RP, Guiochon-Mantel A, Young J. Bouligand J, et al. N Engl J Med. 2009 Jun 25;360(26):2742-8. doi: 10.1056/NEJMoa0900136. Epub 2009 Jun 17. N Engl J Med. 2009. PMID: 19535795 Free article.
[GNRH1 mutation in familial hypogonadotropic hypogonadism].
Bouligand J, Guiochon-Mantel A, Young J. Bouligand J, et al. Med Sci (Paris). 2009 Oct;25(10):791-3. doi: 10.1051/medsci/20092510791. Med Sci (Paris). 2009. PMID: 19849976 Free article. French. No abstract available.
97 results