fbn1 mutation
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A case of G1013R FBN1 mutation: A potential genotype–phenotype correlation in severe Marfan syndrome
2020 ◽
Vol 182
(6)
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pp. 1329-1335
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2018 ◽
Vol 26
(11)
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pp. 2631-2637
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2017 ◽
Vol 16
(5)
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pp. 7321-7328
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