Further patient with Angelman syndrome due to paternal disomy of chromosome 15 and a milder phenotype
- 15 April 1995
- journal article
- letter
- Published by Wiley in American Journal of Medical Genetics
- Vol. 56 (3), 328-329
- https://doi.org/10.1002/ajmg.1320560324
Abstract
No abstract availableThis publication has 9 references indexed in Scilit:
- Detection of aberrant DNA methylation in unique Prader — Willi syndrome patients and its diagnostic implicationsHuman Molecular Genetics, 1994
- Angelman syndrome due to paternal uniparental disomy of chromosome 15: A milder phenotype?American Journal of Medical Genetics, 1994
- Molecular mechanisms in Angelman syndrome: a survey of 93 patients.Journal of Medical Genetics, 1993
- Paternal uniparental disomy in a child with a balanced 15;15 translocation and Angelman syndromeAmerican Journal of Medical Genetics, 1993
- Increased Parental Ages and Uniparental Disomy 15: A Paternal Age Effect?European Journal of Human Genetics, 1993
- Paternal uniparental disomy of chromosome 15 in a child with angelman syndromeAnnals of Neurology, 1992
- The Frequency of Uniparental Disomy in Prader-Willi SyndromeNew England Journal of Medicine, 1992
- Prader–Willi Syndrome and Angelman Syndrome in Cousins from a Family with a Translocation between Chromosomes 6 and 15New England Journal of Medicine, 1992
- Uniparental paternal disomy in Angelman's syndromeThe Lancet, 1991