Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome
Annemieke J.M.H. Verkerk(Erasmus University Rotterdam), Stephen T. Warren(Emory University), Catherine B. Kunst(Erasmus University Rotterdam), Bert E. Eussen(Erasmus University Rotterdam), Orly Reiner(Weizmann Institute of Science), Gert‐Jan B. van Ommen(Leiden University Medical Center), Gregory J. Riggins(Unknown), Maura Pieretti(Howard Hughes Medical Institute), Derek P.A. Kuhl(Howard Hughes Medical Institute), Antonio Pizzuti(Casa Sollievo della Sofferenza), David L. Nelson(Smithsonian Conservation Biology Institute), James S. Sutcliffe(Vanderbilt University), Fuping Zhang(University of Helsinki), Ying‐Hui Fu(Howard Hughes Medical Institute), Lau A.J. Blonden, Ben A. Oostra(Erasmus MC), H. Galjaard(Erasmus University Rotterdam), Jane L. Chastain(Emory University), M F Victoria(Howard Hughes Medical Institute), C. Thomas Caskey(Baylor College of Medicine), Stephen Richards(George Washington University)
Cited by 3,505
Related Papers
Mutations of the BRAF gene in human cancer
|Nature|2002|10.7k
Detection of Circulating Tumor DNA in Early- and Late-Stage Human Malignancies
|Science Translational Medicine|2014|5.1k
Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox
|Cell|1991|2.1k