An Extensive de novo deletion removing FMR1 in a patient with mental retardation and the fragile X syndrome phenotype
- 1 November 1993
- journal article
- case report
- Published by Oxford University Press (OUP) in Human Molecular Genetics
- Vol. 2 (11), 1973-1974
- https://doi.org/10.1093/hmg/2.11.1973