Co-expression of FBN1 with mesenchyme-specific genes in mouse cell lines: implications for phenotypic variability in Marfan syndrome
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Link
http://www.nature.com/articles/ejhg201091.pdf
Reference50 articles.
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2. Pyeritz RE : The Marfan syndrome. Annu Rev Med 2000; 51: 481–510.
3. De Paepe A, Devereux RB, Dietz HC, Hennekam RC, Pyeritz RE : Revised diagnostic criteria for the Marfan syndrome. Am J Med Genet 1996; 62: 417–426.
4. Summers KM, West JA, Peterson MM, Stark D, McGill JJ, West MJ : Challenges in the diagnosis of Marfan syndrome. Med J Aust 2006; 184: 627–631.
5. Dietz HC, Loeys B, Carta L, Ramirez F : Recent progress towards a molecular understanding of Marfan syndrome. Am J Med Genet C Semin Med Genet 2005; 139C: 4–9.
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