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

Year Number of Results
2010 6
2011 5
2012 12
2013 8
2014 7
2015 13
2016 5
2017 6
2018 9
2019 10
2020 7
2021 10
2022 4
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93 results
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Page 1
JP-HHT phenotype in Danish patients with SMAD4 mutations.
Jelsig AM, Tørring PM, Kjeldsen AD, Qvist N, Bojesen A, Jensen UB, Andersen MK, Gerdes AM, Brusgaard K, Ousager LB. Jelsig AM, et al. Clin Genet. 2016 Jul;90(1):55-62. doi: 10.1111/cge.12693. Epub 2015 Dec 21. Clin Genet. 2016. PMID: 26572829
Myhre syndrome.
Le Goff C, Michot C, Cormier-Daire V. Le Goff C, et al. Clin Genet. 2014 Jun;85(6):503-13. doi: 10.1111/cge.12365. Epub 2014 Apr 2. Clin Genet. 2014. PMID: 24580733 Review.
93 results