Dads and disomy and disease
- 1 June 1991
- journal article
- Published by Springer Nature in Nature
- Vol. 351 (6328) , 609-610
- https://doi.org/10.1038/351609a0
Abstract
No abstract availableThis publication has 12 references indexed in Scilit:
- Embryological and molecular investigations of parental imprinting on mouse chromosome 7Nature, 1991
- Uniparental paternal disomy in a genetic cancer-predisposing syndromeNature, 1991
- Parental imprinting of the mouse H19 geneNature, 1991
- The mouse insulin-like growth factor type-2 receptor is imprinted and closely linked to the Tme locusNature, 1991
- 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
- Molecular nature of genetic changes resulting in loss of heterozygosity of chromosome 11 in Wilms' tumoursHuman Genetics, 1988
- Clinical and cytogenetic survey of 39 individuals with Prader‐Labhart‐Willi syndromeAmerican Journal of Medical Genetics, 1986
- Insulin-like growth factor-II gene expression in Wilms' tumour and embryonic tissuesNature, 1985
- Expression of insulin-like growth factor-II transcripts in Wilms' tumourNature, 1985