C278F mutation in FGFR2 gene causes two different types of syndromic craniosynostosis in two Chinese patients.
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Novel chromosomal microduplications associated with dolichocephaly craniosynostosis: A case report.Clinical and next-generation sequencing findings in a Chinese family exhibiting severe familial exudative vitreoretinopathy.Genetic variations in Bestrophin‑1 and associated clinical findings in two Chinese patients with juvenile‑onset and adult‑onset best vitelliform macular dystrophy.
P2860
C278F mutation in FGFR2 gene causes two different types of syndromic craniosynostosis in two Chinese patients.
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2017 nî lūn-bûn
@nan
2017年の論文
@ja
2017年論文
@yue
2017年論文
@zh-hant
2017年論文
@zh-hk
2017年論文
@zh-mo
2017年論文
@zh-tw
2017年论文
@wuu
2017年论文
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2017年论文
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name
C278F mutation in FGFR2 gene c ...... tosis in two Chinese patients.
@en
C278F mutation in FGFR2 gene c ...... tosis in two Chinese patients.
@nl
type
label
C278F mutation in FGFR2 gene c ...... tosis in two Chinese patients.
@en
C278F mutation in FGFR2 gene c ...... tosis in two Chinese patients.
@nl
prefLabel
C278F mutation in FGFR2 gene c ...... tosis in two Chinese patients.
@en
C278F mutation in FGFR2 gene c ...... tosis in two Chinese patients.
@nl
P2093
P2860
P356
P1476
C278F mutation in FGFR2 gene c ...... tosis in two Chinese patients.
@en
P2093
Bingqian Liu
Chenjin Jin
Chuan Chen
Hongbin Gao
Hongye Jiang
Jacob V P Eswarakumar
P2860
P304
P356
10.3892/MMR.2017.7248
P577
2017-08-14T00:00:00Z