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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2009 1
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2012 1
2014 2
2015 3
2016 4
2017 2
2018 1
2020 2
2021 1
2022 0
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Page 1
A Novel SEMA3G Mutation in Two Siblings Affected by Syndromic GnRH Deficiency.
Oleari R, André V, Lettieri A, Tahir S, Roth L, Paganoni A, Eberini I, Parravicini C, Scagliotti V, Cotellessa L, Bedogni F, De Martini LB, Corridori MV, Gulli S, Augustin HG, Gaston-Massuet C, Hussain K, Cariboni A. Oleari R, et al. Among authors: andre v. Neuroendocrinology. 2021;111(5):421-441. doi: 10.1159/000508375. Epub 2020 May 4. Neuroendocrinology. 2021. PMID: 32365351 Free article.
The molecular control of GnRH neuron development.
Cariboni A, Valentina A, Davidson K, Parnavelas J. Cariboni A, et al. Among authors: valentina a. Springerplus. 2015 Jun 12;4(Suppl 1):L46. doi: 10.1186/2193-1801-4-S1-L46. eCollection 2015. Springerplus. 2015. PMID: 27386208 Free PMC article. No abstract available.
IGSF10 mutations dysregulate gonadotropin-releasing hormone neuronal migration resulting in delayed puberty.
Howard SR, Guasti L, Ruiz-Babot G, Mancini A, David A, Storr HL, Metherell LA, Sternberg MJ, Cabrera CP, Warren HR, Barnes MR, Quinton R, de Roux N, Young J, Guiochon-Mantel A, Wehkalampi K, André V, Gothilf Y, Cariboni A, Dunkel L. Howard SR, et al. Among authors: andre v. EMBO Mol Med. 2016 Jun 1;8(6):626-42. doi: 10.15252/emmm.201606250. Print 2016 Jun. EMBO Mol Med. 2016. PMID: 27137492 Free PMC article.
14 results