(Q83220763)
Statements
Detection of 53 FBN1 mutations (41 novel and 12 recurrent) and genotype-phenotype correlations in 113 unrelated probands referred with Marfan syndrome, or a related fibrillinopathy (English)
C L S Turner
H Emery
A L Collins
R J Howarth
C M Yearwood
E Cross
P J Duncan
D J Bunyan
J F Harvey