Detection of full fragile X mutation
Open Access
- 1 February 1992
- journal article
- Published by Elsevier in The Lancet
- Vol. 339 (8788) , 271-272
- https://doi.org/10.1016/0140-6736(92)91334-5
Abstract
No abstract availableKeywords
This publication has 7 references indexed in Scilit:
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- Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndromePublished by Elsevier ,1991
- Instability of a 550-Base Pair DNA Segment and Abnormal Methylation in Fragile X SyndromeScience, 1991
- Physical mapping across the fragile X: Hypermethylation and clinical expression of the fragile X syndromeCell, 1991
- Unusual presentation of fragile X syndromeThe Lancet, 1990