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1. 25: A MULTICENTER COHORT ANALYSIS OF RAPID GENOME SEQUENCING IN THE PICU. (15th December 2022)

2. De novo heterozygous missense and loss‐of‐function variants in CDC42BPB are associated with a neurodevelopmental phenotype. Issue 5 (7th February 2020)

3. Genotype–phenotype correlation at codon 1740 of SETD2. Issue 9 (24th July 2020)

6. Molecular characterization of HDAC8 deletions in individuals with atypical Cornelia de Lange syndrome. Issue 3 (March 2018)

8. Piloting of a minimum data set for older people living in care homes in England: protocol for a longitudinal, mixed-methods study. Issue 2 (27th February 2023)