Kate B. Clarkson

Albright hereditary osteodystrophy and del(2)(q37.3) in four unrelated individuals

Mary C. Phelan, R. Curtis Rogers, Kate B. Clarkson et al. · American Journal of Medical Genetics · 1995 · 132 citations

Cornelia de Lange syndrome in diverse populations

Leah Dowsett, Antonio R. Porras, Paul Kruszka et al. · American Journal of Medical Genetics Part A · 2019 · 53 citations · Full text

Autoimmune Disease, Ophthalmology, Scleroderma +15

17p13.3 microduplications are associated with split-hand/foot malformation and long-bone deficiency (SHFLD)

Christine M. Armour, Dennis E. Bulman, Olga Jarinova et al. · European Journal of Human Genetics · 2011 · 37 citations · Full text

Bone Disease, Musculoskeletal Research, Distraction Osteogenesis +8

A Novel <i>GLRA1</i> Mutation Associated with An Atypical Hyperekplexia Phenotype

Mary Lee Gregory, Gregory F. Guzauskas, Terence S. Edgar et al. · Journal of Child Neurology · 2008 · 16 citations

Engineering, Family Members, Genetics +16