D.I. Rodenhiser

Identification and characterization of sporadic and inherited mutations in exon 31 of the neurofibromatosis (NF1) gene

P J Ainsworth, D.I. Rodenhiser, Maria Teresa Pereira Costa · Human Genetics · 1993 · 48 citations

Mendelian Disorder, Neurogenomics, Genetic Disorder +10

Heterogenous point mutations in the BRCA1 breast cancer susceptibility gene occur in high frequency at the site of homonucleotide tracts, short repeats and methylatable CpG/CpNpG motifs.

D.I. Rodenhiser, Partha Pratim Chakraborty, Joseph Andrews et al. · PubMed · 1996 · 36 citations

A genetic study of neurofibromatosis type 1 (NF1) in south-western Ontario. II. A PCR based approach to molecular and prenatal diagnosis using linkage.

D.I. Rodenhiser, P J Ainsworth, Marion B. Coulter-Mackie et al. · Journal of Medical Genetics · 1993 · 25 citations · Full text

Family Members, Genetics, Genetic Epidemiology +17

A genetic study of neurofibromatosis 1 in south-western Ontario. I. Population, familial segregation of phenotype, and molecular linkage.

D.I. Rodenhiser, Marion B. Coulter-Mackie, Jin-Kyu Jung et al. · Journal of Medical Genetics · 1991 · 21 citations · Full text

Genetics, Genetic Epidemiology, South-western Ontario +18