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

Year Number of Results
1975 1
1992 1
1996 1
1998 1
2001 2
2004 4
2005 3
2006 5
2007 4
2008 6
2009 4
2010 8
2011 8
2012 5
2013 6
2014 8
2015 9
2016 7
2017 17
2018 12
2019 15
2020 27
2021 32
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Article type
Publication date

Similar articles for PMID: 27502037

158 results
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Page 1
Congenital Hypogonadotropic Hypogonadism with Anosmia and Gorlin Features Caused by a PTCH1 Mutation Reveals a New Candidate Gene for Kallmann Syndrome.
Barraud S, Delemer B, Poirsier-Violle C, Bouligand J, Mérol JC, Grange F, Higel-Chaufour B, Decoudier B, Zalzali M, Dwyer AA, Acierno JS, Pitteloud N, Millar RP, Young J. Barraud S, et al. Neuroendocrinology. 2021;111(1-2):99-114. doi: 10.1159/000506640. Epub 2020 Feb 20. Neuroendocrinology. 2021. PMID: 32074614
158 results