A splicing switch and gain-of-function mutation in FgfR2-IIIc hemizygotes causes Apert/Pfeiffer-syndrome-like phenotypes

Mohammad K. Hajihosseini, Stephen Wilson, Laurence De Moerlooze, Clive Dickson

Research output: Contribution to journalArticle

133 Citations (Scopus)
Original languageEnglish
Pages (from-to)3855-3860
Number of pages6
JournalProceedings of the National Academy of Sciences
Volume98
Issue number7
DOIs
Publication statusPublished - 2001

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