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

Year Number of Results
1966 1
1984 2
1990 4
1991 4
1992 7
1993 20
1994 30
1995 18
1996 16
1997 23
1998 15
1999 16
2000 12
2001 13
2002 9
2003 14
2004 14
2005 3
2006 14
2007 19
2008 12
2009 16
2010 17
2011 15
2012 17
2013 12
2014 10
2015 14
2016 14
2017 14
2018 15
2019 12
2020 8
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2022 12
2023 6
2024 0

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Similar articles for PMID: 7738200

420 results

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Page 1
The FBN1 (R2726W) mutation is not fully penetrant.
Buoni S, Zannolli R, Macucci F, Ansaldi S, Grasso M, Arbustini E, Fois A. Buoni S, et al. Ann Hum Genet. 2004 Nov;68(Pt 6):633-8. doi: 10.1046/j.1529-8817.2004.00113.x. Ann Hum Genet. 2004. PMID: 15598221
Skeletal manifestations of Marfan syndrome associated to heterozygous R2726W FBN1 variant: sibling case report and literature review.
Reyes-Hernández OD, Palacios-Reyes C, Chávez-Ocaña S, Cortés-Malagón EM, Alonso-Themann PG, Ramos-Cano V, Ramírez-Bello J, Sierra-Martínez M. Reyes-Hernández OD, et al. BMC Musculoskelet Disord. 2016 Feb 15;17:79. doi: 10.1186/s12891-016-0935-9. BMC Musculoskelet Disord. 2016. PMID: 26875674 Free PMC article. Review.
420 results