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Publications by Lisa Bradley
Bi-Allelic Loss-Of-Function CACNA1B Mutations in Progressive Epilepsy-Dyskinesia
American Journal of Human Genetics
Genetics
Heterozygous Variants in KMT2E Cause a Spectrum of Neurodevelopmental Disorders and Epilepsy
American Journal of Human Genetics
Genetics
Neonatal Lethal Costello Syndrome and Unusual Dinucleotide Deletion/Insertion Mutations in HRAS Predicting p.Gly12Val
American Journal of Medical Genetics, Part A
Genetics
GP239 Case Report: An Irish Male With Bilateral Fibular Aplasia Tibial Campomelia and Oligosyndactyly (FATCO) Syndrome
