Mutation Analysis of theMEN1Gene in Multiple Endocrine Neoplasia Type 1, Familial Acromegaly and Familial Isolated Hyperparathyroidism1
Year: 1998
Type: article
Study design: Observational Study
Authors: B. T. Teh, S. Kytölä, F. Farnebo, L. Bergman, F. K. Wong, G. Weber, N. Hayward, C. Larsson, B. Skogseid, A. Beckers, C. Phelan, M. Edwards, M. Epstein, F. Alford, D. Hurley, S. Grimmond, G. Silins, M. Walters, C. Stewart, J. Cardinal, S. Khodaei, F. Parente, L. Tranebjærg, R. Jorde, J. Menon, A. Khir, T. T. Tan, S. P. Chan, A. Zaini, B. A. K. Khalid, K. Sandelin, N. Thompson, M.-L. Brandi, M. Warth, J. Stock, J. Leisti, D. Cameron, J. J. Shepherd, K. Öberg, M. Nordenskjöld, P. Salmela
Institutions: Karolinska University Hospital, Karolinska Institutet, QIMR Berghofer Medical Research Institute, Uppsala University Hospital, University of Liège, Centre Hospitalier Universitaire de Liège, Royal Perth Hospital, University Hospital of North Norway, Queen Elizabeth Hospital, University of Malaya, National University of Malaysia, Michigan Medicine, University of Florence, Royal Hobart Hospital, Oulu University Hospital
Language: English
Subfield: Epidemiology
Field: Medicine
Domain: Health Sciences
Open Access status: closed
OpenAlex ID: W2113007209