Relevance of genomic imprinting to human diseases
- 31 December 1992
- journal article
- review article
- Published by Elsevier in Current Opinion in Biotechnology
- Vol. 3 (6) , 632-636
- https://doi.org/10.1016/0958-1669(92)90007-6
Abstract
No abstract availableKeywords
This publication has 27 references indexed in Scilit:
- Beckwith-wiedemann syndrome, tumourigenesis and imprintingCurrent Opinion in Genetics & Development, 1992
- The Frequency of Uniparental Disomy in Prader-Willi SyndromeNew England Journal of Medicine, 1992
- Implications of genomic imprinting for psychiatric geneticsPsychological Medicine, 1992
- The syntenic relationship between the critical deletion region for the Prader-Willi/Angelman syndromes and proximal mouse chromosome 7Genomics, 1991
- Uniparental disomy, isodisomy, and imprinting: Probable effects in man and strategies for their detectionAmerican Journal of Medical Genetics, 1991
- Genomic imprinting in an Angelman and Prader-Willi translocation familyThe Lancet, 1991
- Genomic imprintingCurrent Opinion in Genetics & Development, 1991
- DIFFERENTIAL IMPRINTING AND EXPRESSION OF MATERNAL AND PATERNAL GENOMESAnnual Review of Genetics, 1988
- Differential activity of maternally and paternally derived chromosome regions in miceNature, 1985
- Completion of mouse embryogenesis requires both the maternal and paternal genomesCell, 1984