Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome
- 31 May 1991
- journal article
- Published by Elsevier BV in Cell
- Vol. 65 (5), 905-914
- https://doi.org/10.1016/0092-8674(91)90397-h
Abstract
No abstract availableKeywords
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