FBN1 mutation screening of patients with Marfan syndrome and related disorders: detection of 46 novel FBN1 mutations
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.2008.01007.x/fullpdf
Reference36 articles.
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2. Revised genomic organization of FBN1 and significance for regulated gene expression;Biery;Genomics,1999
3. Genomic organization of the sequence coding for fibrillin, the defective gene product in Marfan syndrome;Pereira;Hum Mol Genet,1993
4. Partial sequence of a candidate gene for the Marfan syndrome;Maslen;Nature,1991
5. The molecular genetics of Marfan syndrome and related disorders;Robinson;J Med Genet,2006
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