Similar articles for PMID: 21936929

Year	Number of Results
1993	1
1994	3
1995	1
1996	2
2000	3
2001	7
2002	6
2004	2
2005	3
2006	12
2007	11
2008	5
2009	11
2010	13
2011	19
2012	19
2013	19
2014	19
2015	7
2016	9
2017	9
2018	6
2019	10
2020	7
2021	10
2022	15
2023	6
2024	0

1

Characterization of large genomic deletions in the FBN1 gene using multiplex ligation-dependent probe amplification.

Furtado LV, Wooderchak-Donahue W, Rope AF, Yetman AT, Lewis T, Plant P, Bayrak-Toydemir P. Furtado LV, et al. BMC Med Genet. 2011 Sep 21;12:119. doi: 10.1186/1471-2350-12-119. BMC Med Genet. 2011. PMID: 21936929 Free PMC article.

2

The spectrum of FBN1, TGFβR1, TGFβR2 and ACTA2 variants in 594 individuals with suspected Marfan Syndrome, Loeys-Dietz Syndrome or Thoracic Aortic Aneurysms and Dissections (TAAD).

Lerner-Ellis JP, Aldubayan SH, Hernandez AL, Kelly MA, Stuenkel AJ, Walsh J, Joshi VA. Lerner-Ellis JP, et al. Mol Genet Metab. 2014 Jun;112(2):171-6. doi: 10.1016/j.ymgme.2014.03.011. Epub 2014 Apr 2. Mol Genet Metab. 2014. PMID: 24793577

3

Genotype-phenotype analysis of F-helix mutations at the kinase domain of TGFBR2, including a type 2 Marfan syndrome familial study.

Zhang L, Gao LG, Zhang M, Zhou XL. Zhang L, et al. Mol Vis. 2012;18:55-63. Epub 2012 Jan 11. Mol Vis. 2012. PMID: 22259224 Free PMC article.

4

Identification of novel FBN1 and TGFBR2 mutations in 65 probands with Marfan syndrome or Marfan-like phenotypes.

Chung BH, Lam ST, Tong TM, Li SY, Lun KS, Chan DH, Fok SF, Or JS, Smith DK, Yang W, Lau YL. Chung BH, et al. Am J Med Genet A. 2009 Jul;149A(7):1452-9. doi: 10.1002/ajmg.a.32918. Am J Med Genet A. 2009. PMID: 19533785

5

Comparison of clinical presentations and outcomes between patients with TGFBR2 and FBN1 mutations in Marfan syndrome and related disorders.

Attias D, Stheneur C, Roy C, Collod-Béroud G, Detaint D, Faivre L, Delrue MA, Cohen L, Francannet C, Béroud C, Claustres M, Iserin F, Khau Van Kien P, Lacombe D, Le Merrer M, Lyonnet S, Odent S, Plauchu H, Rio M, Rossi A, Sidi D, Steg PG, Ravaud P, Boileau C, Jondeau G. Attias D, et al. Circulation. 2009 Dec 22;120(25):2541-9. doi: 10.1161/CIRCULATIONAHA.109.887042. Epub 2009 Dec 7. Circulation. 2009. PMID: 19996017 Free article.

6

Genetic Risk for Aortic Aneurysm in Adolescent Idiopathic Scoliosis.

Haller G, Alvarado DM, Willing MC, Braverman AC, Bridwell KH, Kelly M, Lenke LG, Luhmann SJ, Gurnett CA, Dobbs MB. Haller G, et al. J Bone Joint Surg Am. 2015 Sep 2;97(17):1411-7. doi: 10.2106/JBJS.O.00290. J Bone Joint Surg Am. 2015. PMID: 26333736 Free PMC article.

7

Large genomic fibrillin-1 (FBN1) gene deletions provide evidence for true haploinsufficiency in Marfan syndrome.

Mátyás G, Alonso S, Patrignani A, Marti M, Arnold E, Magyar I, Henggeler C, Carrel T, Steinmann B, Berger W. Mátyás G, et al. Hum Genet. 2007 Aug;122(1):23-32. doi: 10.1007/s00439-007-0371-x. Epub 2007 May 10. Hum Genet. 2007. PMID: 17492313 Free article.

8

Marfan syndrome type II: there is more to Marfan syndrome than fibrillin 1.

Zangwill SD, Brown MD, Bryke CR, Cava JR, Segura AD. Zangwill SD, et al. Congenit Heart Dis. 2006 Sep;1(5):229-32. doi: 10.1111/j.1747-0803.2006.00040.x. Congenit Heart Dis. 2006. PMID: 18377530

9

Comprehensive genetic analysis of relevant four genes in 49 patients with Marfan syndrome or Marfan-related phenotypes.

Sakai H, Visser R, Ikegawa S, Ito E, Numabe H, Watanabe Y, Mikami H, Kondoh T, Kitoh H, Sugiyama R, Okamoto N, Ogata T, Fodde R, Mizuno S, Takamura K, Egashira M, Sasaki N, Watanabe S, Nishimaki S, Takada F, Nagai T, Okada Y, Aoka Y, Yasuda K, Iwasa M, Kogaki S, Harada N, Mizuguchi T, Matsumoto N. Sakai H, et al. Am J Med Genet A. 2006 Aug 15;140(16):1719-25. doi: 10.1002/ajmg.a.31353. Am J Med Genet A. 2006. PMID: 16835936

10

Identification of gross deletions in FBN1 gene by MLPA.

Yang H, Ma Y, Luo M, Zhao K, Zhang Y, Zhu G, Sun X, Luo F, Wang L, Shu C, Zhou Z. Yang H, et al. Hum Genomics. 2018 Oct 4;12(1):46. doi: 10.1186/s40246-018-0178-y. Hum Genomics. 2018. PMID: 30286810 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Results by year

Text availability

Article attribute

Article type

Publication date

206 results

Results by year