I. Biroš

Frequency of spinocerebellar ataxia types 1, 2, 3, 6, and 7 in Australian patients with spinocerebellar ataxia

Elsdon Storey, Desirée du Sart, Janet Shaw et al. · American Journal of Medical Genetics · 2000 · 97 citations

Spinal muscular atrophy: untangling the knot?

I. Biroš, Susan Forrest · Journal of Medical Genetics · 1999 · 71 citations · Full text

Genetics, Molecular Genetics, Spine Deformity +16

Two cases of prenatal analysis for the pathogenic T to G substitution at nucleotide 8993 in mitochondrial DNA

S. L. White, Sara Shanske, I. Biroš et al. · Prenatal Diagnosis · 1999 · 64 citations

Genetics, Genetic Epidemiology, Molecular Genetics +21

The second generation of the International Equine Gene Mapping Workshop half‐sibling linkage map

G. Guérin, Ernest Bailey, D Bernoco et al. · Animal Genetics · 2003 · 51 citations

Biology, Linkage Disequilibrium, Second Generation Map +15

Polymorphism of the p53 gene within the codon 72 in lung cancer patients.

Erik Biroš, I Kalina, I. Biroš et al. · PubMed · 2001 · 31 citations

Genetics, Genetic Epidemiology, Human Polymorphism +17