Double mutant fibrillin-1 (FBN1) allele in a patient with neonatal Marfan syndrome. [electronic resource]

By: Contributor(s): Producer: 19970204Description: 760-3 p. digitalISSN:
  • 0022-2593
Subject(s): Online resources: In: Journal of medical genetics vol. 33
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Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.

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