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Year | Number of Results |
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2007 | 1 |
2012 | 2 |
2020 | 1 |
2024 | 0 |
PubMed (cited) for id: 614897
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Functional analysis of SEMA3A variants identified in Chinese patients with isolated hypogonadotropic hypogonadism.
Clin Genet. 2020 May;97(5):696-703. doi: 10.1111/cge.13723. Epub 2020 Feb 21.
Clin Genet. 2020.
PMID: 32060892
SEMA3A, a gene involved in axonal pathfinding, is mutated in patients with Kallmann syndrome.
Hanchate NK, Giacobini P, Lhuillier P, Parkash J, Espy C, Fouveaut C, Leroy C, Baron S, Campagne C, Vanacker C, Collier F, Cruaud C, Meyer V, García-Piñero A, Dewailly D, Cortet-Rudelli C, Gersak K, Metz C, Chabrier G, Pugeat M, Young J, Hardelin JP, Prevot V, Dodé C.
Hanchate NK, et al.
PLoS Genet. 2012 Aug;8(8):e1002896. doi: 10.1371/journal.pgen.1002896. Epub 2012 Aug 23.
PLoS Genet. 2012.
PMID: 22927827
Free PMC article.
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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.
Hum Reprod. 2012 May;27(5):1460-5. doi: 10.1093/humrep/des022. Epub 2012 Mar 12.
Hum Reprod. 2012.
PMID: 22416012
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Reversal of idiopathic hypogonadotropic hypogonadism.
Raivio T, Falardeau J, Dwyer A, Quinton R, Hayes FJ, Hughes VA, Cole LW, Pearce SH, Lee H, Boepple P, Crowley WF Jr, Pitteloud N.
Raivio T, et al.
N Engl J Med. 2007 Aug 30;357(9):863-73. doi: 10.1056/NEJMoa066494.
N Engl J Med. 2007.
PMID: 17761590
Free article.
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