Revisiting Crouzon syndrome: reviewing the background and management of a multifaceted disease.
about
Analysis of the Fgfr2C342Y mouse model shows condensation defects due to misregulation of Sox9 expression in prechondrocytic mesenchyme.Selective mutation accumulation: a computational model of the paternal age effect.Mutation c.943G>T (p.Ala315Ser) in FGFR2 Causing a Mild Phenotype of Crouzon Craniofacial Dysostosis in a Three-Generation Family.Sleep-related hypermotor epilepsy in a patient with mild Crouzon syndrome.C-type natriuretic peptide analog treatment of craniosynostosis in a Crouzon syndrome mouse modelUltrasound and MR imaging findings in prenatal diagnosis of craniosynostosis syndromes
P2860
Revisiting Crouzon syndrome: reviewing the background and management of a multifaceted disease.
description
2014 nî lūn-bûn
@nan
2014年の論文
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2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
@wuu
2014年论文
@zh
2014年论文
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name
Revisiting Crouzon syndrome: r ...... ent of a multifaceted disease.
@en
type
label
Revisiting Crouzon syndrome: r ...... ent of a multifaceted disease.
@en
prefLabel
Revisiting Crouzon syndrome: r ...... ent of a multifaceted disease.
@en
P2860
P1476
Revisiting Crouzon syndrome: r ...... ent of a multifaceted disease.
@en
P2093
Sameep Kadakia
Samuel N Helman
P2860
P2888
P304
P356
10.1007/S10006-014-0467-0
P577
2014-09-24T00:00:00Z