Dorothy Trump

Clinical studies of multiple endocrine neoplasia type 1 (MEN1)

Dorothy Trump, Bernadette Farren, C Wooding et al. · QJM · 1996 · 469 citations · Full text

Calcium-sensing receptor mutations in familial benign hypercalcemia and neonatal hyperparathyroidism.

Simon H. S. Pearce, Dorothy Trump, C Wooding et al. · Journal of Clinical Investigation · 1995 · 349 citations · Full text

Car Gene, Developmental Biology, Neonatal Hyperparathyroidism +13

3q29 Microdeletion Syndrome: Clinical and Molecular Characterization of a New Syndrome

Lionel Willatt, James J. Cox, John Barber et al. · The American Journal of Human Genetics · 2005 · 295 citations · Full text

Molecular Characterization, Gene Deletion Data, Genetic Disorder +10

Perrault Syndrome Is Caused by Recessive Mutations in CLPP, Encoding a Mitochondrial ATP-Dependent Chambered Protease

Emma M. Jenkinson, Atteeq U. Rehman, Tom Walsh et al. · The American Journal of Human Genetics · 2013 · 238 citations · Full text

Mitochondrial Function, Genetic Disorder, Medicine +7

Molecular characterisation of <i>SMARCB1</i> and <i>NF2</i> in familial and sporadic schwannomatosis

Kristin Hadfield, William G. Newman, Naomi L. Bowers et al. · Journal of Medical Genetics · 2008 · 204 citations