Similar articles for PMID: 11170092

Year	Number of Results
1992	1
1993	3
1994	8
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1996	2
1997	5
1998	2
1999	1
2000	4
2001	8
2002	6
2003	4
2004	4
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2006	4
2007	8
2008	4
2009	2
2010	2
2011	3
2012	2
2013	3
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2016	1
2022	2
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1

Characterization of microsatellite markers flanking FBN1: utility in the diagnostic evaluation for Marfan syndrome.

Judge DP, Biery NJ, Dietz HC. Judge DP, et al. Am J Med Genet. 2001 Feb 15;99(1):39-47. doi: 10.1002/1096-8628(20010215)99:1<39::aid-ajmg1114>3.0.co;2-3. Am J Med Genet. 2001. PMID: 11170092

2

Genotype and phenotype analysis of 171 patients referred for molecular study of the fibrillin-1 gene FBN1 because of suspected Marfan syndrome.

Loeys B, Nuytinck L, Delvaux I, De Bie S, De Paepe A. Loeys B, et al. Arch Intern Med. 2001 Nov 12;161(20):2447-54. doi: 10.1001/archinte.161.20.2447. Arch Intern Med. 2001. PMID: 11700157

3

De novo 15q21.1q21.2 deletion identified through FBN1 MLPA and refined by 244K array-CGH in a female teenager with incomplete Marfan syndrome.

Faivre L, Khau Van Kien P, Callier P, Ruiz-Pallares N, Baudoin C, Plancke A, Wolf JE, Thauvin-Robinet C, Durand E, Minot D, Dulieu V, Metaizeau JD, Leheup B, Coron F, Bidot S, Huet F, Jondeau G, Boileau C, Claustres M, Mugneret F. Faivre L, et al. Eur J Med Genet. 2010 Jul-Aug;53(4):208-12. doi: 10.1016/j.ejmg.2010.05.002. Epub 2010 May 15. Eur J Med Genet. 2010. PMID: 20478419

4

[AFBN1 gene in patients with Marfan syndrome].

Valiev RR, Khusainova RI, Kutuev IA, Khusnutdinova EK. Valiev RR, et al. Mol Biol (Mosk). 2006 Nov-Dec;40(6):1021-30. Mol Biol (Mosk). 2006. PMID: 17209430 Russian.

5

[Indirect genotype analysis as a diagnostic procedure in Marfan syndrome].

Laudahn BM, Gyürüs P, Orth U, Gal A, Nienaber CA. Laudahn BM, et al. Z Kardiol. 2000 Oct;89(10):939-48. doi: 10.1007/s003920070168. Z Kardiol. 2000. PMID: 11098545 German.

6

Allelic frequencies of FBN1 gene polymorphisms and genetic analysis of italian families with Marfan syndrome.

Mottes M, Mirandola S, Rigatelli F, Zolezzi F, Lisi V, Gordon D, Pignatti PF. Mottes M, et al. Hum Hered. 2000 May-Jun;50(3):175-9. doi: 10.1159/000022910. Hum Hered. 2000. PMID: 10686496

7

Classic, atypically severe and neonatal Marfan syndrome: twelve mutations and genotype-phenotype correlations in FBN1 exons 24-40.

Tiecke F, Katzke S, Booms P, Robinson PN, Neumann L, Godfrey M, Mathews KR, Scheuner M, Hinkel GK, Brenner RE, Hövels-Gürich HH, Hagemeier C, Fuchs J, Skovby F, Rosenberg T. Tiecke F, et al. Eur J Hum Genet. 2001 Jan;9(1):13-21. doi: 10.1038/sj.ejhg.5200582. Eur J Hum Genet. 2001. PMID: 11175294

8

DNA diagnostics of the Marfan syndrome: application of amplifiable polymorphic markers.

Rantamäki T, Lönnqvist L, Karttunen L, Kainulainen K, Peltonen L. Rantamäki T, et al. Eur J Hum Genet. 1994;2(1):66-75. doi: 10.1159/000472343. Eur J Hum Genet. 1994. PMID: 8044654

9

FBN1 mutation in Chinese patients with Marfan syndrome and its gene diagnosis using haplotype linkage analysis.

Wang B, Hu D, Xia J, Li Q, Yang J, Lu G. Wang B, et al. Chin Med J (Engl). 2003 Jul;116(7):1043-6. Chin Med J (Engl). 2003. PMID: 12890380

10

Correlation of a recurrent FBN1 mutation (R122C) with an atypical familial Marfan syndrome phenotype.

Black C, Withers AP, Gray JR, Bridges AB, Craig A, Baty DU, Boxer M. Black C, et al. Hum Mutat. 1998;Suppl 1:S198-200. doi: 10.1002/humu.1380110164. Hum Mutat. 1998. PMID: 9452085 No abstract available.

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