Collaborative prospective study of the fragile X syndrome: One‐year progress report
Year: 1992
Type: article
Study design: Observational Study
Authors: S. L. Sherman, G. Barbi, K. Brøndum‐Nielsen, W. T. Brown, N. J. Carpenter, A. E. Chudley, O. P. Ferraz, P. Ferreira, K‐H. Gustavson, J. Halliday, A. Hockey, P. N. Howard‐Peebles, E. Jenkins, I. Kennerknecht, M. Kähkönen, P. Ladaïque, J. Leisti, A. Maddalena, T. Mazurczak, J‐F. Mattei, T. Mattina, M. J. McKinley, P. Murphy, M. C. Pellissier, S. Purvis‐Smith, H. Robinson, U. Scapagnini, T. Schaap, L. R. Shapiro, A. P. T. Smits, P. Steinbach, G. Turner, I. A. Uchida, B. A. Van Oost, M‐A. Voelckel, D. D. Weaver, T. Webb
Institutions: Emory University, Universität Ulm, Children's Hospital of Winnipeg, Instituto Butantan, University of Alberta, University of Alberta Hospital, Uppsala University, Government of Western Australia Department of Health, Virginia Commonwealth University Medical Center, Oulu University Hospital, Hôpital de la Timone, Instytut Matki i Dziecka, University of Catania, Churchill Hospital, New York State Department of Health, Prince of Wales Hospital, Oasi Maria SS, Hadassah Medical Center, New York Medical College, McMaster University, Indiana University School of Medicine, Indiana University, Birmingham Women's Hospital
Language: English
Subfield: Genetics
Domain: Life Sciences
Open Access status: closed
OpenAlex ID: W2116846102