Similar articles for PMID: 11285249

Year	Number of Results
1991	1
1992	1
1993	2
1994	5
1995	9
1996	8
1997	7
1998	6
1999	8
2000	6
2001	5
2002	7
2003	4
2004	4
2005	4
2006	5
2007	4
2008	2
2009	5
2010	11
2011	6
2012	9
2013	9
2014	8
2015	8
2016	4
2017	1
2018	3
2019	7
2020	9
2021	6
2022	11
2023	2
2024	0

1

Mutation of the gene encoding fibrillin-2 results in syndactyly in mice.

Chaudhry SS, Gazzard J, Baldock C, Dixon J, Rock MJ, Skinner GC, Steel KP, Kielty CM, Dixon MJ. Chaudhry SS, et al. Hum Mol Genet. 2001 Apr 1;10(8):835-43. doi: 10.1093/hmg/10.8.835. Hum Mol Genet. 2001. PMID: 11285249

2

Fibrillin-2 (FBN2) mutations result in the Marfan-like disorder, congenital contractural arachnodactyly.

Putnam EA, Zhang H, Ramirez F, Milewicz DM. Putnam EA, et al. Nat Genet. 1995 Dec;11(4):456-8. doi: 10.1038/ng1295-456. Nat Genet. 1995. PMID: 7493032

3

Clustering of FBN2 mutations in patients with congenital contractural arachnodactyly indicates an important role of the domains encoded by exons 24 through 34 during human development.

Park ES, Putnam EA, Chitayat D, Child A, Milewicz DM. Park ES, et al. Am J Med Genet. 1998 Jul 24;78(4):350-5. Am J Med Genet. 1998. PMID: 9714438

4

Ten novel FBN2 mutations in congenital contractural arachnodactyly: delineation of the molecular pathogenesis and clinical phenotype.

Gupta PA, Putnam EA, Carmical SG, Kaitila I, Steinmann B, Child A, Danesino C, Metcalfe K, Berry SA, Chen E, Delorme CV, Thong MK, Adès LC, Milewicz DM. Gupta PA, et al. Hum Mutat. 2002 Jan;19(1):39-48. doi: 10.1002/humu.10017. Hum Mutat. 2002. PMID: 11754102

5

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.

6

ENU mutagenesis reveals a novel phenotype of reduced limb strength in mice lacking fibrillin 2.

Miller G, Neilan M, Chia R, Gheryani N, Holt N, Charbit A, Wells S, Tucci V, Lalanne Z, Denny P, Fisher EM, Cheeseman M, Askew GN, Dear TN. Miller G, et al. PLoS One. 2010 Feb 9;5(2):e9137. doi: 10.1371/journal.pone.0009137. PLoS One. 2010. PMID: 20161761 Free PMC article.

7

Mutations in the human gene for fibrillin-1 (FBN1) in the Marfan syndrome and related disorders.

Dietz HC, Pyeritz RE. Dietz HC, et al. Hum Mol Genet. 1995;4 Spec No:1799-809. doi: 10.1093/hmg/4.suppl_1.1799. Hum Mol Genet. 1995. PMID: 8541880 Review.

8

Of mice and Marfan: genetic linkage analyses of the fibrillin genes, Fbn1 and Fbn2, in the mouse genome.

Goldstein C, Liaw P, Jimenez SA, Buchberg AM, Siracusa LD. Goldstein C, et al. Mamm Genome. 1994 Nov;5(11):696-700. doi: 10.1007/BF00426075. Mamm Genome. 1994. PMID: 7873879

9

Comprehensive clinical and molecular assessment of 32 probands with congenital contractural arachnodactyly: report of 14 novel mutations and review of the literature.

Callewaert BL, Loeys BL, Ficcadenti A, Vermeer S, Landgren M, Kroes HY, Yaron Y, Pope M, Foulds N, Boute O, Galán F, Kingston H, Van der Aa N, Salcedo I, Swinkels ME, Wallgren-Pettersson C, Gabrielli O, De Backer J, Coucke PJ, De Paepe AM. Callewaert BL, et al. Hum Mutat. 2009 Mar;30(3):334-41. doi: 10.1002/humu.20854. Hum Mutat. 2009. PMID: 19006240 Review.

10

Two novel fibrillin-2 mutations in congenital contractural arachnodactyly.

Belleh S, Zhou G, Wang M, Der Kaloustian VM, Pagon RA, Godfrey M. Belleh S, et al. Am J Med Genet. 2000 May 1;92(1):7-12. Am J Med Genet. 2000. PMID: 10797416

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