Genotype and phenotype in Angelman syndrome caused by paternal UPD 15
- 13 June 1997
- journal article
- letter
- Published by Wiley in American Journal of Medical Genetics
- Vol. 70 (3) , 328-329
- https://doi.org/10.1002/(sici)1096-8628(19970613)70:3<328::aid-ajmg21>3.0.co;2-m
Abstract
No abstract availableThis publication has 9 references indexed in Scilit:
- Angelman syndromeCurrent Problems in Pediatrics, 1995
- Further patient with Angelman syndrome due to paternal disomy of chromosome 15 and a milder phenotypeAmerican Journal of Medical Genetics, 1995
- Angelman syndrome due to paternal uniparental disomy of chromosome 15: A milder phenotype?American Journal of Medical Genetics, 1994
- Familial unbalanced translocation t(8;15)(p23.3;q11) with uniparental disomy in Angelman syndromeHuman Genetics, 1994
- Paternal uniparental disomy in a child with a balanced 15;15 translocation and Angelman syndromeAmerican Journal of Medical Genetics, 1993
- Paternal uniparental disomy of chromosome 15 in a child with angelman syndromeAnnals of Neurology, 1992
- Maternal but not paternal transmission of 15q11–13–linked nondeletion Angelman syndrome leads to phenotypic expressionNature Genetics, 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