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

Year Number of Results
1993 3
2001 2
2002 3
2003 5
2004 5
2005 4
2006 6
2007 4
2008 11
2009 3
2010 7
2011 10
2012 10
2013 10
2014 8
2015 10
2016 13
2017 11
2018 7
2019 8
2020 11
2021 13
2022 12
2023 10
2024 0

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PubMed for id: 201163

162 results

Results by year

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Page 1
Genetic insight into Birt-Hogg-Dubé syndrome in Indian patients reveals novel mutations at FLCN.
Ray A, Chattopadhyay E, Singh R, Ghosh S, Bera A, Sarma M, Munot M, Desai U, Rajan S, Prabhudesai P, Prakash AK, Roy Chowdhury S, Bhowmick N, Dhar R, Udwadia ZF, Dey A, Mitra S, Joshi JM, Maitra A, Roy B. Ray A, et al. Orphanet J Rare Dis. 2022 Apr 27;17(1):176. doi: 10.1186/s13023-022-02326-5. Orphanet J Rare Dis. 2022. PMID: 35477461 Free PMC article.
A retrospective two centre study of Birt-Hogg-Dubé syndrome reveals a pathogenic founder mutation in FLCN in the Swedish population.
Lagerstedt-Robinson K, Baranowska Körberg I, Tsiaprazis S, Björck E, Tham E, Poluha A, Hellström Pigg M, Paulsson-Karlsson Y, Nordenskjöld M, Johansson-Soller M, Aravidis C. Lagerstedt-Robinson K, et al. PLoS One. 2022 Feb 17;17(2):e0264056. doi: 10.1371/journal.pone.0264056. eCollection 2022. PLoS One. 2022. PMID: 35176117 Free PMC article.
162 results