Molecular diagnosis of the Prader-Willi and Angelman syndromes by detection of parent-of-origin specific DNA methylation in 15q11-13
- 1 November 1992
- journal article
- research article
- Published by Springer Nature in Human Genetics
- Vol. 90 (3), 313-315
- https://doi.org/10.1007/bf00220089
Abstract
No abstract availableKeywords
This publication has 9 references indexed in Scilit:
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- Microdissection of the Prader-Willi syndrome chromosome region and identification of potential gene sequencesGenomics, 1990
- Genetic imprinting suggested by maternal heterodisomy in non-deletion Prader-Willi syndromeNature, 1989
- The association of Angelman's syndrome with deletions within 15q11-13.Journal of Medical Genetics, 1989
- Angelman and Prader‐Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletionAmerican Journal of Medical Genetics, 1989
- Deletions of Chromosome 15 as a Cause of the Prader–Willi SyndromeNew England Journal of Medicine, 1981