Orest Hurko

Severe achondroplasia with developmental delay and acanthosis nigricans (SADDAN): phenotypic analysis of a new skeletal dysplasia caused by a Lys650Met mutation in fibroblast growth factor receptor 3.

M. Bamshad, E. Jabs, J. Dorst, 1999, American journal of medical genetics.

Directly repeated sequences associated with pathogenic mitochondrial DNA deletions.

O. C. Stine, O. Hurko, D. Johns, 1989, Proceedings of the National Academy of Sciences of the United States of America.

Disorders of binocular control of eye movements in patients with cerebellar dysfunction.

D. Zee, M. Versino, O. Hurko, 1996, Brain : a journal of neurology.

Association between Ag1-CA alleles and severity of autosomal recessive proximal spinal muscular atrophy.

J. McPherson, J. Carpten, B. Wirth, 1994, American journal of human genetics.

Preferential amplification and molecular characterization of junction sequences of a pathogenetic deletion in human mitochondrial DNA.

O. Hurko, D. Johns, Orest Hurko, 1989, Genomics.

Craniocervical decompression for cervicomedullary compression in pediatric patients with achondroplasia.

B. Carson, C. Francomano, O. Hurko, 1990, Journal of neurosurgery.