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Displaying the 1 most recent scholarly work by Julie Cayrol.
Wilms Tumor Associated With the 9q22.3 Microdeletion Syndrome: 2 New Case Reports and a Review of The Literature
Julie Cayrol, Michael Nightingale, Jacqueline Challis, Martin Campbell, Michael Sullivan, Yves Heloury
Journal article | 2019 | Journal of Pediatric Hematology/Oncology
BACKGROUND: The 9q22.3 syndrome is an autosomal dominant microdeletion syndrome with similarities to Gorlin syndrome (GS). It enco..
Paediatrics Royal Children's Hospital