Harold G. Marks

Dejerine–Sottas syndrome associated with point mutation in the peripheral myelin protein 22 (PMP22) gene

Benjamin B. Roa, P. James B. Dyck, Harold G. Marks et al. · Nature Genetics · 1993 · 254 citations

Mendelian Disorder, Neurological Disorder, Genetic Disorder +9

Recessive TTN truncating mutations define novel forms of core myopathy with heart disease

Claire Chauveau, Carsten G. Bönnemann, Cédric Julien et al. · Human Molecular Genetics · 2013 · 187 citations · Full text

Dystrophinopathy in isolated cases of myopathy in females

Eric P. Hoffman, Kiichi Arahata, Carlo Minetti et al. · Neurology · 1992 · 161 citations

Gynecology, Pathology, Orthopaedic Surgery +19

The CNS phenotype of X-linked Charcot-Marie-Tooth disease

Robert A. Taylor, Erin M. Simon, Harold G. Marks et al. · Neurology · 2003 · 145 citations

Neurological Disorder, X-linked Charcot-marie-tooth Disease, Pathology +16

Detection of new paternal dystrophin gene mutations in isolated cases of dystrophinopathy in females.

Elena Pegoraro, R. Neil Schimke, Kiichi Arahata et al. · PubMed · 1994 · 142 citations