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Keyword [Apert syndrome]
Result: 1 - 8 | Page: 1 of 1
1.
Study On Pathogenesis Of Apert Syndrome Caused By Fgfr2 Gain-of-function Mutation
2.
Comparable Study On Craniofacial Maldevelopment In Apert Syndrome Patients And FGFR2-S252W P253R Mouse Model
3.
Influence Of Fgfr2Gain-of-function Mutation On The Mandible And Teeth Of Mice
4.
Study On Bone Mass And Bone Marrow Mesenchymal Stem Cells Of Osteogenic Differentiation Regulation Mechanism In The Apert Syndrome FGFR
S252W/+
Mice
5.
Study On The Development Of Endochondral Bone Formation Caused By FGFR2Gain-of-fuction Mouse In Early Postnatal Stage
6.
Apert Syndrome Disease Gene FGFR2E731K Mutation On Osteoblast Differentiation And MVs Mineralization
7.
Morphological Analysis Of Craniofacial Deformities In Crouzon Syndrome And Apert Syndrome
8.
The Mechanisms Of Skull Deformation And Molecular Therapy In Apert Syndrome
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