DOI:
10.1055/s-00000034
Klinische Pädiatrie
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References
Haywood J, Rae A, Porteous M, Logie L, Brock D.
Two novel mutations and a neutral polymorphism in the EGF-like domains of the fibrillin gene (FBN1): SSCP screening of exons 15 - 21 in Marfan syndrome patients.
Hum Mol Genet 1994; 3: 373-375
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