New molecular mechanisms of craniosynostosis
Lead Research Organisation:
UNIVERSITY OF OXFORD
Department Name: RDM Radcliffe Department of Medicine
Abstract
Abstracts are not currently available in GtR for all funded research. This is normally because the abstract was not required at the time of proposal submission, but may be because it included sensitive information such as personal details.
Organisations
People |
ORCID iD |
| Andrew O M Wilkie (Primary Supervisor) | |
| Rebecca Tooze (Student) |
Publications
Tooze RS
(2023)
Craniosynostosis, inner ear, and renal anomalies in a child with complete loss of SPRY1 (sprouty homolog 1) function.
in Journal of medical genetics
Hyder Z
(2021)
Evaluating the performance of a clinical genome sequencing program for diagnosis of rare genetic disease, seen through the lens of craniosynostosis.
in Genetics in medicine : official journal of the American College of Medical Genetics
Studentship Projects
| Project Reference | Relationship | Related To | Start | End | Student Name |
|---|---|---|---|---|---|
| MR/N013468/1 | 30/09/2016 | 29/09/2025 | |||
| 2271075 | Studentship | MR/N013468/1 | 30/09/2019 | 29/09/2023 | Rebecca Tooze |