A case of
G1013R
FBN1
mutation: A potential
genotype–phenotype
correlation in severe Marfan syndrome
2020 ◽
Vol 182
(6)
◽
pp. 1329-1335
Keyword(s):
2006 ◽
Vol 39
(2)
◽
pp. 171-183
◽
Keyword(s):
2016 ◽
Vol 37
(43)
◽
pp. 3291-3293
◽