Authors: MEIJER H DEGRAAFF E MERCKX DML JONGBLOED RJE DEDIESMULDERS CEM ENGELEN JJM FRYNS JP CURFS PMG OOSTRA BA

Citation: H. Meijer et al., A DELETION OF 1.6 KB PROXIMAL TO THE CGG REPEAT OF THE FMR1 GENE CAUSES THE CLINICAL PHENOTYPE OF THE FRAGILE X SYNDROME, Human molecular genetics, 3(4), 1994, pp. 615-620