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Publication | Open Access

Correlation of a recurrent FBN1 mutation (R122C) with an atypical familial marfan syndrome phenotype

DOIFull Paper Access

28

Citations

12

References

1998

Year

Cheryl Black, Anne P. Withers, Jonathon Gray, Allan B. Bridges, Ashley Craig, David Baty, Maureen Boxer
Human Mutation

References

YearCitations

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