Examinant per Autoria "Corbett, Mark A."
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Ítem Accés Obert Genomic and phenotypic characterization of 404 individuals with neurodevelopmental disorders caused by CTNNB1 variants(Elsevier, 2022) Kayumi, Sayaka; Pérez Jurado, Luis Alberto; Corbett, Mark A.
Ítem Accés Obert Pathogenic copy number variants that affect gene expression contribute to genomic burden in cerebral palsy(Nature Research, 2018) Corbett, Mark A.; van Eyk, Clare L.; Webber, Dani L.; Bent, Stephen J.; Newman, Morgan; Harper, Kelly; Berry, Jesia G.; Azmanov, Dimitar N.; Woodward, Karen J.; Gardner, Alison E.; Slee, Jennie; Pérez Jurado, Luis Alberto; MacLennan, Alastair H.; Gecz, Jozef
Ítem Accés Obert Yield of clinically reportable genetic variants in unselected cerebral palsy by whole genome sequencing(Nature Research, 2021) van Eyk, Clare L.; Webber, Dani L.; Minoche, André E.; Pérez Jurado, Luis Alberto; Corbett, Mark A.; Gardner, Alison E.; Berry, Jesia G.; Harper, Kelly; MacLennan, Alastair H.; Gecz, Jozef