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

Year Number of Results
1995 1
2001 3
2004 1
2005 3
2006 4
2007 6
2008 11
2009 6
2010 13
2011 14
2012 9
2013 13
2014 12
2015 8
2016 6
2017 10
2018 6
2019 8
2020 13
2021 24
2022 26
2023 9
2024 0

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Similar articles for PMID: 22035731

181 results

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Page 1
Nasal embryonic LHRH factor (NELF) mutations in patients with normosmic hypogonadotropic hypogonadism and Kallmann syndrome.
Xu N, Kim HG, Bhagavath B, Cho SG, Lee JH, Ha K, Meliciani I, Wenzel W, Podolsky RH, Chorich LP, Stackhouse KA, Grove AM, Odom LN, Ozata M, Bick DP, Sherins RJ, Kim SH, Cameron RS, Layman LC. Xu N, et al. Fertil Steril. 2011 Apr;95(5):1613-20.e1-7. doi: 10.1016/j.fertnstert.2011.01.010. Epub 2011 Feb 15. Fertil Steril. 2011. PMID: 21300340 Free PMC article.
Identification of HESX1 mutations in Kallmann syndrome.
Newbern K, Natrajan N, Kim HG, Chorich LP, Halvorson LM, Cameron RS, Layman LC. Newbern K, et al. Fertil Steril. 2013 Jun;99(7):1831-7. doi: 10.1016/j.fertnstert.2013.01.149. Epub 2013 Mar 1. Fertil Steril. 2013. PMID: 23465708 Free PMC article.
181 results