Philip Stanier

4PUBLICATIONS
9CO-AUTHORS
Developmental genetics (incl. sex determination)NeurogeneticsCancer therapy (excl. chemotherapy and radiation therapy)Rehabilitation engineering
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Publications (4)

|Jun 25, 2019
Analysis of transgenic zebrafish expressing the Lenz-Majewski syndrome gene PTDSS1 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 Fgfr2c 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