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An extensive de novo deletion removing FMR1 in a patient with mental retardation and the fragile X syndrome phenotype.
- Source :
-
Human molecular genetics [Hum Mol Genet] 1993 Nov; Vol. 2 (11), pp. 1973-4. - Publication Year :
- 1993
Details
- Language :
- English
- ISSN :
- 0964-6906
- Volume :
- 2
- Issue :
- 11
- Database :
- MEDLINE
- Journal :
- Human molecular genetics
- Publication Type :
- Academic Journal
- Accession number :
- 8281165
- Full Text :
- https://doi.org/10.1093/hmg/2.11.1973