Similar articles for PMID: 8317497

Year	Number of Results
1955	1
1983	1
1991	4
1992	3
1993	9
1994	13
1995	3
1996	4
1997	7
1998	1
1999	2
2000	8
2001	4
2002	7
2003	2
2004	4
2005	3
2006	3
2007	2
2008	1
2009	3
2011	2
2012	3
2013	3
2014	2
2015	4
2016	2
2017	1
2021	3
2023	1
2024	0

1

Autosomal dominant Marfan-like connective-tissue disorder with aortic dilation and skeletal anomalies not linked to the fibrillin genes.

Boileau C, Jondeau G, Babron MC, Coulon M, Alexandre JA, Sakai L, Melki J, Delorme G, Dubourg O, Bonaïti-Pellié C, et al. Boileau C, et al. Am J Hum Genet. 1993 Jul;53(1):46-54. Am J Hum Genet. 1993. PMID: 8317497 Free PMC article.

2

A rare branch-point mutation is associated with missplicing of fibrillin-2 in a large family with congenital contractural arachnodactyly.

Maslen C, Babcock D, Raghunath M, Steinmann B. Maslen C, et al. Am J Hum Genet. 1997 Jun;60(6):1389-98. doi: 10.1086/515472. Am J Hum Genet. 1997. PMID: 9199560 Free PMC article.

3

Fibrillin-1 mutations in Marfan syndrome and other type-1 fibrillinopathies.

Hayward C, Brock DJ. Hayward C, et al. Hum Mutat. 1997;10(6):415-23. doi: 10.1002/(SICI)1098-1004(1997)10:6<415::AID-HUMU1>3.0.CO;2-C. Hum Mutat. 1997. PMID: 9401003 Review.

4

Linkage of Marfan syndrome and a phenotypically related disorder to two different fibrillin genes.

Lee B, Godfrey M, Vitale E, Hori H, Mattei MG, Sarfarazi M, Tsipouras P, Ramirez F, Hollister DW. Lee B, et al. Nature. 1991 Jul 25;352(6333):330-4. doi: 10.1038/352330a0. Nature. 1991. PMID: 1852206

5

[The Marfan syndrome and related connective tissue disorders].

Siepe M, Löffelbein F. Siepe M, et al. Med Monatsschr Pharm. 2009 Jun;32(6):213-9. Med Monatsschr Pharm. 2009. PMID: 19554831 Review. German.

6

The molecular genetics of Marfan syndrome and related microfibrillopathies.

Robinson PN, Godfrey M. Robinson PN, et al. J Med Genet. 2000 Jan;37(1):9-25. doi: 10.1136/jmg.37.1.9. J Med Genet. 2000. PMID: 10633129 Free PMC article. Review.

7

A second locus for Marfan syndrome maps to chromosome 3p24.2-p25.

Collod G, Babron MC, Jondeau G, Coulon M, Weissenbach J, Dubourg O, Bourdarias JP, Bonaïti-Pellié C, Junien C, Boileau C. Collod G, et al. Nat Genet. 1994 Nov;8(3):264-8. doi: 10.1038/ng1194-264. Nat Genet. 1994. PMID: 7632217 Free PMC article.

8

Clinical and genetic associations in Marfan syndrome and related disorders.

Ramirez F, Lee B, Vitale E. Ramirez F, et al. Mt Sinai J Med. 1992 Sep;59(4):350-6. Mt Sinai J Med. 1992. PMID: 1406753

9

Genetic linkage of the Marfan syndrome, ectopia lentis, and congenital contractural arachnodactyly to the fibrillin genes on chromosomes 15 and 5. The International Marfan Syndrome Collaborative Study.

Tsipouras P, Del Mastro R, Sarfarazi M, Lee B, Vitale E, Child AH, Godfrey M, Devereux RB, Hewett D, Steinmann B, et al. Tsipouras P, et al. N Engl J Med. 1992 Apr 2;326(14):905-9. doi: 10.1056/NEJM199204023261401. N Engl J Med. 1992. PMID: 1542340 Free article.

10

Fibrillin genes map to regions of conserved mouse/human synteny on mouse chromosomes 2 and 18.

Li X, Pereira L, Zhang H, Sanguineti C, Ramirez F, Bonadio J, Francke U. Li X, et al. Genomics. 1993 Dec;18(3):667-72. doi: 10.1016/s0888-7543(05)80371-4. Genomics. 1993. PMID: 8307578 Free article.

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