Joseph K Park

Reciprocal and nonreciprocal recombination at the glucocerebrosidase gene region: implications for complexity in Gaucher disease.

Ellen Sidransky, E. Sidransky, N. Tayebi, 2003, American journal of human genetics.

Myoclonic Epilepsy in Gaucher Disease: Genotype-Phenotype Insights from a Rare Patient Subgroup

R. Schiffmann, B. Martin, E. Sidransky, 2003, Pediatric Research.

Phenotypic continuum in neuronopathic Gaucher disease: an intermediate phenotype between type 2 and type 3.

R. Schiffmann, E. Sidransky, O. Goker-Alpan, 2003, The Journal of pediatrics.

Glucosylsphingosine accumulation in tissues from patients with Gaucher disease: correlation with phenotype and genotype.

E. Ginns, B. Martin, E. Sidransky, 2002, Molecular genetics and metabolism.

A deletion-insertion mutation in the phosphomannomutase 2 gene in an African American patient with congenital disorders of glycosylation-Ia.

D. Krasnewich, E. Sidransky, N. Tayebi, 2002, American journal of medical genetics.

Gene rearrangement on 1q21 introducing a duplication of the glucocerebrosidase pseudogene and a metaxin fusion gene

E. Sidransky, N. Tayebi, Joseph K Park, 2000, Human Genetics.