Riyana Babul

Frequency of spinocerebellar ataxia type 1, dentatorubropallidoluysian atrophy, and Machado-Joseph disease mutations in a large group of spinocerebellar ataxia patients

Isabel Silveira, Íscia Lopes‐Cendes, Stephen J. Kish et al. · Neurology · 1996 · 105 citations

Attitudes toward direct predictive testing for the Huntington disease gene. Relevance for other adult-onset disorders. The Canadian Collaborative Group on Predictive Testing for Huntington Disease.

Riyana Babul, Shelin Adam, B Kremer et al. · PubMed · 1993 · 69 citations

Omphalocele in Miller-Dieker syndrome: Expanding the phenotype

David Chitayat, Ants Toi, Riyana Babul et al. · American Journal of Medical Genetics · 1997 · 38 citations

Normal Male Karyotype, Genetics, Pathology +17

Prenatal diagnosis of retinal nonattachment in the Walker‐Warburg syndrome

David Chitayat, Ants Toi, Riyana Babul et al. · American Journal of Medical Genetics · 1995 · 32 citations

Limits of Clinical Assessment in the Accurate Diagnosis of Machado-Joseph Disease

Íscia Lopes‐Cendes, Isabel Silveira, Patrı́cia Maciel et al. · Archives of Neurology · 1996 · 32 citations