p.Ser252Trp and p.Pro253Arg mutations in FGFR2 gene causing Apert syndrome: the first clinical and molecular report of Indonesian patients

F.E.P. Mundhofir, E.A. Sistermans, S.M.H. Faradz, B.C.J. Hamel

Research output: Contribution to journalArticleAcademicpeer-review

Original languageUndefined/Unknown
Pages (from-to)E72-E75
JournalSingapore medical journal
Volume54
Issue number3
DOIs
Publication statusPublished - 2013

Cite this