Detection of minimum mutation carriers in myotonic dystrophy
- 25 July 1992
- journal article
- other
- Published by Elsevier in The Lancet
- Vol. 340 (8813), 238-239
- https://doi.org/10.1016/0140-6736(92)90501-s
Abstract
No abstract availableThis publication has 8 references indexed in Scilit:
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- Population screening for fragile XThe Lancet, 1992
- Cloning of the essential myotonic dystrophy region and mapping of the putative defectNature, 1992
- Detection of an unstable fragment of DNA specific to individuals with myotonic dystrophyNature, 1992
- Expansion of an unstable DNA region and phenotypic variation in myotonic dystrophyNature, 1992
- Molecular basis of myotonic dystrophy: Expansion of a trinucleotide (CTG) repeat at the 3′ end of a transcript encoding a protein kinase family memberCell, 1992
- Detection of full fragile X mutationThe Lancet, 1992
- Genealogical reconstruction of myotonic dystrophy in the Saguenay‐Lac‐Saint‐ Jean area (Quebec, Canada)Neurology, 1990