Rebecca S Tooze

2PUBLICATIONS
5CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Neonatology
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Publications (2)

|Mar 29, 2023
Review of Recurrently Mutated Genes in Craniosynostosis Supports Expansion of Diagnostic Gene Panels.

Rebecca S Tooze, Eduardo Calpena, Astrid Weber

|Dec 21, 2022
Craniosynostosis, inner ear, and renal anomalies in a child with complete loss of SPRY1 (sprouty homolog 1) function.

Rebecca S Tooze, Eduardo Calpena, Stephen R F Twigg

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Frequent Collaborators

2 joint publications

Eduardo Calpena

2 joint publications

Stephen R F Twigg

2 joint publications

Andrew O M Wilkie

1 joint publications

Felice D'Arco