Prenatal diagnosis of myotonic dystrophy by direct mutation analysis
- 25 July 1992
- journal article
- other
- Published by Elsevier in The Lancet
- Vol. 340 (8813) , 237-238
- https://doi.org/10.1016/0140-6736(92)90500-3
Abstract
No abstract availableThis publication has 7 references indexed in Scilit:
- Identification of variable simple sequence motifs in 19q13.2-qter: Markers for the myotonic dystrophy locusPublished by Elsevier ,2004
- An Unstable Triplet Repeat in a Gene Related to Myotonic Muscular DystrophyScience, 1992
- Myotonic Dystrophy Mutation: an Unstable CTG Repeat in the 3′ Untranslated region of the GeneScience, 1992
- Molecular basis of myotonic dystrophy: Expansion of a trinucleotide (CTG) repeat at the 3′ end of a transcript encoding a protein kinase family memberPublished by Elsevier ,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