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

Year Number of Results
1960 1
1980 1
1981 1
1984 1
1986 1
1988 3
1990 2
1992 4
1993 5
1994 4
1995 7
1996 6
1997 8
1998 8
1999 3
2000 5
2001 8
2002 6
2003 5
2004 6
2005 1
2006 6
2007 5
2008 6
2010 1
2011 3
2012 5
2013 5
2014 5
2015 3
2016 5
2017 3
2018 6
2019 5
2020 6
2021 3
2022 5
2023 0
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146 results
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Page 1
Germline variants in HEY2 functional domains lead to congenital heart defects and thoracic aortic aneurysms.
van Walree ES, Dombrowsky G, Jansen IE, Umićević Mirkov M, Zwart R, Ilgun A, Guo D, Clur SB, Amin AS, Savage JE, van der Wal AC, Waisfisz Q, Maugeri A, Wilsdon A, Bu'Lock FA, Hurles ME, Dittrich S, Berger F, Audain Martinez E, Christoffels VM, Hitz MP, Milewicz DM, Posthuma D, Meijers-Heijboer H, Postma AV, Mathijssen IB. van Walree ES, et al. Among authors: zwart r. Genet Med. 2022 Apr;24(4):965. doi: 10.1016/j.gim.2022.01.018. Genet Med. 2022. PMID: 35394427 No abstract available.
PRDM10 directs FLCN expression in a novel disorder overlapping with Birt-Hogg-Dubé syndrome and familial lipomatosis.
van de Beek I, Glykofridis IE, Oosterwijk JC, Akker PC, Diercks GFH, Bolling MC, Waisfisz Q, Mensenkamp AR, Balk JA, Zwart R, Postma AV, Meijers-Heijboer HEJ, Moorselaar RJA, Wolthuis RMF, Houweling AC. van de Beek I, et al. Among authors: zwart r. Hum Mol Genet. 2022 Nov 28:ddac288. doi: 10.1093/hmg/ddac288. Online ahead of print. Hum Mol Genet. 2022. PMID: 36440963
146 results