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

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@article{9b152faeb74d46a999e6a5614cb0ce9f,

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

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

year = "2013",

doi = "https://doi.org/10.11622/smedj.2013055",

language = "English",

volume = "54",

pages = "E72--E75",

journal = "Singapore medical journal",

issn = "0037-5675",

publisher = "Singapore Medical Association",

number = "3",

}

TY - JOUR

T1 - p.Ser252Trp and p.Pro253Arg mutations in FGFR2 gene causing Apert syndrome: the first clinical and molecular report of Indonesian patients

AU - Mundhofir, F.E.P.

AU - Sistermans, E.A.

AU - Faradz, S.M.H.

AU - Hamel, B.C.J.

PY - 2013

Y1 - 2013

U2 - https://doi.org/10.11622/smedj.2013055

DO - https://doi.org/10.11622/smedj.2013055

M3 - Article

SN - 0037-5675

VL - 54

SP - E72-E75

JO - Singapore medical journal

JF - Singapore medical journal

IS - 3

ER -