Matthew Wakeling
0000-0002-6542-9241
4 papers found
Refreshing results…
Paediatric diabetes subtypes in a consanguineous population: a single-centre cohort study from Kurdistan, Iraq
A biallelic loss‐of‐function PDIA6 variant in a second patient with polycystic kidney disease, infancy‐onset diabetes, and microcephaly
SavvyCNV: Genome-wide CNV calling from off-target reads
Refinement of the critical genomic region for congenital hyperinsulinism in the Chromosome 9p deletion syndrome
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