Signalling paradigms of fibroblast growth factor receptor type 2 : studies from a Crouzon-Pfeiffer syndrome mouse model
Main Author: | Perlyn, Chad |
---|---|
Published: |
University of Oxford
2006
|
Subjects: | |
Online Access: | http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.433337 |
Similar Items
-
The roles of the homeobox genes ALX4 and MSX2 in skull development
by: Mavrogiannis, Lampros A.
Published: (2004) -
Cortical Thickness in Crouzon–Pfeiffer Syndrome: Findings in Relation to Primary Cranial Vault Expansion
by: Alexander T. Wilson, BS, et al.
Published: (2020-10-01) -
Estudo molecular das craniossinostoses sindrômicas: Crouzon, Pfeiffer e Saethre-Chotzen\"
by: Nélio Alessandro de Jesus Oliveira
Published: (2006) -
Estudo molecular das craniossinostoses sindrômicas: Crouzon, Pfeiffer e Saethre-Chotzen\"
by: Oliveira, Nélio Alessandro de Jesus
Published: (2006) -
Crouzon Syndrome: a fibroblast growth factor receptor 2 gene mutation
by: Farhad Safari, et al.
Published: (2017-01-01)