Uniparental disomy as the basis for an association of rare disorders
- 1 November 1991
- journal article
- letter
- Published by Wiley in American Journal of Medical Genetics
- Vol. 41 (2), 273-274
- https://doi.org/10.1002/ajmg.1320410233
Abstract
No abstract availableThis publication has 12 references indexed in Scilit:
- Parental Imprinting of GenesScientific American, 1990
- Prader‐Willi syndrome: Current understanding of cause and diagnosisAmerican Journal of Medical Genetics, 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
- DIFFERENTIAL IMPRINTING AND EXPRESSION OF MATERNAL AND PATERNAL GENOMESAnnual Review of Genetics, 1988
- Chromosome Mapping with DNA MarkersScientific American, 1988
- Coexistence of Prader-Willi syndrome, congenital ectropion uveae with glaucoma, and factor XI deficiencyJAMA, 1986
- LEUKAEMIA AND THE PRADER-WILLI SYNDROMEThe Lancet, 1985
- A new genetic concept: Uniparental disomy and its potential effect, isodisomyAmerican Journal of Medical Genetics, 1980