G.W. Padberg

Localization of the gene for Cowden disease to chromosome 10q22–23

Marcel Nelen, G.W. Padberg, E Peeters et al. · Nature Genetics · 1996 · 669 citations

Cowden Disease, Genetics, Pathogenesis +5

Diagnostic criteria for facioscapulohumeral muscular dystrophy

G.W. Padberg, Peter Lunt, Manuela C. Koch et al. · Neuromuscular Disorders · 1991 · 218 citations

Diagnosis, Motor Disorder, Medicine +3

Clinical features of facioscapulohumeral muscular dystrophy 2

Jessica C. de Greef, Richard J.L.F. Lemmers, Pilar Camaño et al. · Neurology · 2010 · 179 citations · Full text

Linkage of Autosomal Dominant Hearing Loss to the Short Arm of Chromosome 1 in Two Families

Paul Coucke, Guy Van Camp, Bulantrisna Djoyodiharjo et al. · New England Journal of Medicine · 1994 · 135 citations · Full text

Localization of a gene for non-syndromic hearing loss (DFNA5) to chromosome 7p15

Guy Van Camp, Paul Coucke, Wendy Balemans et al. · Human Molecular Genetics · 1995 · 101 citations

Non-syndromic Hearing Loss, Genetics, Genetic Epidemiology +18