The syntenic relationship between the critical deletion region for the Prader-Willi/Angelman syndromes and proximal mouse chromosome 7
- 30 November 1991
- Vol. 11 (3) , 773-776
- https://doi.org/10.1016/0888-7543(91)90090-2
Abstract
No abstract availableKeywords
This publication has 12 references indexed in Scilit:
- PARENTAL ORIGIN OF CHROMOSOME 15 DELETION IN PRADER-WILLI SYNDROMEThe Lancet, 2003
- 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
- Angelman and Prader‐Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletionAmerican Journal of Medical Genetics, 1989
- Similar molecular deletions on chromosome 15q11.2 are encountered in both the Prader-Willi and Angelman syndromesHuman Genetics, 1988
- Is angelman syndrome an alternate result of del(15)(qllql3)?American Journal of Medical Genetics, 1987
- Clinical heterogeneity associated with deletions in the long arm of chromosome 15: Report of 3 new cases and their possible genetic significanceAmerican Journal of Medical Genetics, 1987
- Identification of cDNA clones for the human microtubule-associated protein tau and chromosomal localization of the genes for tau and microtubule-associated protein 2Molecular Brain Research, 1986
- Clinical and cytogenetic survey of 39 individuals with Prader‐Labhart‐Willi syndromeAmerican Journal of Medical Genetics, 1986
- Deletions of Chromosome 15 as a Cause of the Prader–Willi SyndromeNew England Journal of Medicine, 1981