Romesh Khardori

Clinical delineation and localization to chromosome 9p13.3-p12 of a unique dominant disorder in four families: hereditary inclusion body myopathy, Paget disease of bone, and…

Molecular Genetics and Metabolism · 2001 · 165 citations

Clinical and molecular studies in a unique family with autosomal dominant limb-girdle muscular dystrophy and Paget disease of bone

Case report · Genetics in Medicine · 2000 · 115 citations