Instability versus predictability: the molecular diagnosis of myotonic dystrophy.
Open Access
- 1 November 1992
- journal article
- research article
- Published by BMJ in Journal of Medical Genetics
- Vol. 29 (11) , 761-765
- https://doi.org/10.1136/jmg.29.11.761
Abstract
No abstract availableThis publication has 31 references indexed in Scilit:
- Minimal expression of myotonic dystrophy: a clinical and molecular analysis.Journal of Medical Genetics, 1992
- Presymptomatic diagnosis of myotonic dystrophy.Journal of Medical Genetics, 1992
- Specific molecular prenatal diagnosis for the CTG mutation in myotonic dystrophy.Journal of Medical Genetics, 1992
- Fragile X founder effect?Nature Genetics, 1992
- Anal abnormalities in childhood myotonic dystrophy--a possible source of confusion in child sexual abuse.Archives of Disease in Childhood, 1992
- Expansion of unstable DNA region in Japanese myotonic dystrophy patientsThe Lancet, 1992
- Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradoxCell, 1991
- MYOTONIC DYSTROPHYBrain, 1991
- Ethnic distribution of myotonic dystrophy geneThe Lancet, 1991
- Hereditary unstable DNA: a new explanation for some old genetic questions?Published by Elsevier ,1991