FBN2 mutation associated with manifestations of Marfan syndrome and congenital contractural arachnodactyly.

P. A. Gupta, D. D. Wallis, T. O. Chin, H. Northrup, V. T. Tran-Fadulu, Jeffrey Towbin, D. M. Milewicz

Research output: Contribution to journalLetter

44 Citations (Scopus)
Original languageEnglish (US)
JournalJournal of Medical Genetics
Volume41
Issue number5
DOIs
StatePublished - Jan 1 2004
Externally publishedYes

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RNA Splicing
Microfilament Proteins
Marfan Syndrome
Disease Progression
Mutation
Congenital contractural arachnodactyly

All Science Journal Classification (ASJC) codes

  • Genetics
  • Genetics(clinical)

Cite this

FBN2 mutation associated with manifestations of Marfan syndrome and congenital contractural arachnodactyly. / Gupta, P. A.; Wallis, D. D.; Chin, T. O.; Northrup, H.; Tran-Fadulu, V. T.; Towbin, Jeffrey; Milewicz, D. M.

In: Journal of Medical Genetics, Vol. 41, No. 5, 01.01.2004.

Research output: Contribution to journalLetter

Gupta, P. A. ; Wallis, D. D. ; Chin, T. O. ; Northrup, H. ; Tran-Fadulu, V. T. ; Towbin, Jeffrey ; Milewicz, D. M. / FBN2 mutation associated with manifestations of Marfan syndrome and congenital contractural arachnodactyly. In: Journal of Medical Genetics. 2004 ; Vol. 41, No. 5.
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