A deletion of 1.6 kb proximal to the CGG repeat of the FMR1 gene causes the clinical phenotype of the fragile X syndrome.

Published in:

Human Molecular Genetics, 1994, v. 3, n. 4, p. 615

By:

• Meljer, Henk;
• de Graaff, Esther;
• Merckx, Diane M.L.;
• Jongbloed, Roselle J.E.;
• de Die-Smulders, Christine E.M.;
• Engelen, John J.M.;
• Fryns, Jean-Pierre;
• Curfs, Paul M.G.;
• Oostra, Ben A.

Publication type:

Article