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Publications by Deborah Morrogh
Mutations in SNX14 Cause a Distinctive Autosomal-Recessive Cerebellar Ataxia and Intellectual Disability Syndrome
American Journal of Human Genetics
Genetics
Malan Syndrome: Sotos-Like Overgrowth With De Novo NFIX Sequence Variants and Deletions in Six New Patients and a Review of the Literature
European Journal of Human Genetics
Genetics
Inherited Duplications of PPP2R3B Promote Naevi and Melanoma via a Novel C21orf91-Driven Proliferative Phenotype