Shprintzen-Goldberg syndrome results from mutations in fibrillin-1, not monosomy 22q11 [3] (multiple letters)

E. Hatchwell, M. C. Johnson, M. S. Watson, S. B. Dowton, A. W. Strauss

Research output: Contribution to journalLetterpeer-review

5 Scopus citations
Original languageEnglish
Pages (from-to)164-165
Number of pages2
JournalJournal of Pediatrics
Issue number1 I
StatePublished - 1997

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