Genomic imprinting in an Angelman and Prader-Willi translocation family
- 7 September 1991
- journal article
- other
- Published by Elsevier in The Lancet
- Vol. 338 (8767) , 638-639
- https://doi.org/10.1016/0140-6736(91)90652-6
Abstract
No abstract availableKeywords
This publication has 7 references indexed in Scilit:
- Genomic imprinting: developmental significance and molecular mechanismCurrent Opinion in Genetics & Development, 1991
- Uniparental paternal disomy in Angelman's syndromeThe Lancet, 1991
- Maternal origin of 15q11–13 deletions in Angelman syndrome suggests a role for genomic imprintingAmerican Journal of Medical Genetics, 1990
- Comparison of the 15q deletions in Prader‐Willi and Angelman syndromes: Specific regions, extent of deletions, parental origin, and clinical consequencesAmerican Journal of Medical Genetics, 1990
- Prader‐Willi syndrome: Current understanding of cause and diagnosisAmerican Journal of Medical Genetics, 1990
- Prader-Willi syndrome in siblings, due to unbalanced translocation between chromosomes 15 and 22.Archives of Disease in Childhood, 1987
- Genomic imprinting determines methylation of parental alleles in transgenic miceNature, 1987