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The American Journal of Human Genetics, ISSN 0002-9297, 07/2017, Volume 101, Issue 1, pp. 87 - 103
Journal Article
Journal of Medical Genetics, ISSN 0022-2593, 01/1994, Volume 31, Issue 1, pp. 33 - 36
The molecular basis of myotonic dystrophy (DM) has been characterised. All DM mutations characterised to date appear as an unstable elongation of a fragment... 
POPULATION | D19S63 | GENE | MAPS | MARKER | FRAGILE-X SYNDROME | SEQUENCE | GENETICS & HEREDITY | UNSTABLE DNA REGION | LOCUS | Haplotypes | DNA Probes | Gene Frequency | Humans | Alleles | Chromosome Aberrations | Myotonic Dystrophy - genetics | Repetitive Sequences, Nucleic Acid | Mutation | Restriction Mapping | Linkage Disequilibrium | Index Medicus
Journal Article
Human Molecular Genetics, ISSN 0964-6906, 1995, Volume 4, Issue 1, pp. 135 - 136
Journal Article
Journal of Power Sources, ISSN 0378-7753, 11/2016, Volume 331, pp. 32 - 42
Journal Article
PLoS Genetics, ISSN 1553-7390, 2014, Volume 10, Issue 6, pp. e1004299 - e1004299
Journal Article
Journal Article
Injury, ISSN 0020-1383, 2016, Volume 47, Issue 10, pp. 2212 - 2217
Journal Article