Skeletal analysis of the Fgfr3(P244R) mouse, a genetic model for the Muenke craniosynostosis syndrome. (Q54780420)

3 June 2018

title

Skeletal analysis of the Fgfr3(P244R) mouse, a genetic model for the Muenke craniosynostosis syndrome. (English)

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3 June 2018

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Andrew Oliver Mungo Wilkie

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3 June 2018

Paul T Sharpe

object named as

Paul T Sharpe

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author name string

Chris Healy

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3 June 2018

Christian Babbs

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3 June 2018

Jacqueline A Sharpe

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William G Wood

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Gillian M Morriss-Kay

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publication date

1 February 2009

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3 June 2018

published in

Developmental Dynamics

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3 June 2018

volume

238

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3 June 2018

page(s)

331-342

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issue

2

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3 June 2018

Apert syndrome mutations in fibroblast growth factor receptor 2 exhibit increased affinity for FGF ligand

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inferred from DOI database lookup

7 January 2021

based on heuristic

Hearing loss in a mouse model of Muenke syndrome

1 reference

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inferred from DOI database lookup

7 January 2021

based on heuristic

Effects of induced premaxillary suture fusion on the craniofacial morphology in growing rats

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inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1002/DVDY.21790

1 reference

3 June 2018

PubMed ID

19086028

1 reference

3 June 2018