Genetics of Congenital and Acquired Cardiovascular Disease
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Publisher
Springer London
Link
http://link.springer.com/content/pdf/10.1007/978-1-4471-4619-3_89
Reference95 articles.
1. Faivre L, Collod-Beroud G, Child A, Callewaert B, Loeys BL et al (2008) Contribution of molecular analyses in diagnosing Marfan syndrome and type I fibrillinopathies: an international study of 1009 probands. J Med Genet 45:384–390
2. Faivre L, Collod-Beroud G, Loeys BL, Child A, Binquet C et al (2007) Effect of mutation type and location on clinical outcome in 1,013 probands with Marfan syndrome or related phenotypes and FBN1 mutations: an international study. Am J Hum Genet 81:454–466
3. Stheneur C, Collod-Beroud G, Faivre L, Buyck JF, Gouya L et al (2009) Identification of the minimal combination of clinical features in probands for efficient mutation detection in the FBN1 gene. Eur J Hum Genet 17:1121–1128
4. Ng CM, Cheng A, Myers LA, Martinez-Murillo F, Jie C et al (2004) TGF-beta-dependent pathogenesis of mitral valve prolapse in a mouse model of Marfan syndrome. J Clin Invest 114:1586–1592
5. Brooke BS, Habashi JP, Judge DP, Patel N, Loeys B et al (2008) Angiotensin II blockade and aortic-root dilatation in Marfan’s syndrome. N Engl J Med 358:2787–2795
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