Collaborative prospective study of the fragile X syndrome: One‐year progress report

S. L. Sherman(Emory University), T. Webb(Birmingham Women's Hospital), Athel Hockey, David D. Weaver(Indiana University School of Medicine), Stuart Purvis‐Smith(Prince of Wales Hospital), J F Mattei, U. Scapagnini(Oasi Maria SS), Edmund C. Jenkins, Ingo Kennerknecht(University of Münster), Tadeusz Mazurczak(Polish Mother’s Memorial Hospital Research Institute), Peter Steinbach(University Hospital Ulm), Anne Smits(KU Leuven), Jaakko Leisti(Oulu University Hospital), Gotthold Barbi(Universität Ulm), Pedro Ruan Chaves Ferreira(University of Alberta Hospital), Hazel M. Robinson(Blood Cancer UK), Teresa Mattina, Jane Halliday(Northern Health and Social Care Trust), Patricia N. Howard‐Peebles(Genetics and IVF Institute), M. C. Pellissier, Patricia D. Murphy(Newark Beth Israel Medical Center), P. Ladaïque, Irene A. Uchida, Bernard A. van Oost(Radboud University Nijmegen), M‐A. Voelckel, M. Kähkönen(Fimlab (Finland)), K. H. Gustavson(Uppsala University Hospital), N Carpenter(Children's Medical Center), A Maddalena(Virginia Commonwealth University Medical Center), T. Schaap(Hadassah Academic College), W. Ted Brown, Karen Brøndum‐Nielsen(Newcastle University), M. J. McKinley(Churchill Hospital), AE Chudley(Children's Hospital of Winnipeg), L. R. Shapiro(New York Medical College), O. P. Ferraz(Instituto Butantan), Gordon Turner(Prince of Wales Hospital)
American Journal of Medical Genetics
April 15, 1992
Cited by 8


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