Cytogenetic versus DNA diagnosis in routine referrais for fragile X syndrome
- 23 October 1993
- journal article
- Published by Elsevier in The Lancet
- Vol. 342 (8878), 1025-1026
- https://doi.org/10.1016/0140-6736(93)92882-t
Abstract
No abstract availableKeywords
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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 syndromeCell, 1991
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