DOI:
10.1055/s-00029027
Journal of Pediatric Genetics
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References
Faivre L, Collod-Beroud G, Callewaert B. , et al.
Clinical and mutation-type analysis from an international series of 198 probands with a pathogenic FBN1 exons 24-32 mutation.
Eur J Hum Genet 2009;
17 (04) 491-501
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