Philip Stanier
4PUBLICATIONS
9CO-AUTHORS
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Publications (4)
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|Jun 25, 2019
Analysis of transgenic zebrafish expressing the Lenz-Majewski syndrome gene <i>PTDSS1</i> in skeletal cell lineages.Marian Seda, Emma Peskett, Charalambos Demetriou
|Mar 28, 2019
Disruption of FOXF2 as a Likely Cause of Absent Uvula in an Egyptian Family.R Seselgyte, D Bryant, C Demetriou
|Sep 30, 2018
Overexpression of <i>Fgfr2c</i> causes craniofacial bone hypoplasia and ameliorates craniosynostosis in the Crouzon mouse.Kevin K L Lee, Emma Peskett, Charlotte M Quinn
|May 17, 2018
Mice with endogenous TDP-43 mutations exhibit gain of splicing function and characteristics of amyotrophic lateral sclerosis.Pietro Fratta, Prasanth Sivakumar, Jack Humphrey
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Frequent Collaborators
1 joint publications
Pietro Fratta
1 joint publications
Joffrey Mianne
1 joint publications
Adrian M Isaacs
1 joint publications
Nicolas L Fawzi
1 joint publications
Emanuele Buratti
1 joint publications
Abraham Acevedo-Arozena
1 joint publications
Erwin Pauws
1 joint publications
Marian Seda
1 joint publications
Dagan Jenkins
