Slater,Howard Robert

Institution: Royal Children's Hospital, Australia

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

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