Slater,Howard Robert

Institution: Royal Children's Hospital, Australia

Top Collaborators: Ganesamoorthy D, Bruno DL, Amor DJ, White SM, Ngo C, Godler DE, Norris F, Oertel R, Schoumans J, Loesch DZ, Pertile MD, Yeung A, Hagerman RJ, Burgess T, Mcgillivray G, Francis D, Sheffield L, Tan T, Tassone F, Bankier A

Research Interests: Gene, Mutation, Mental Retardation, Microarray Analysis, Time, Epigenetic, Fragile X Syndrome, MALDI, Methylation, Syndrome, Single Nucleotide Polymorphism, Congenital Abnormality, Genome, Syndromes, Ataxia, Cerebellar Ataxia, Families, Gene Deletion, Inositol, Inositol 1,4,5-triphosphate
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