Is there evidence for anticipation in autosomal-dominant polycystic kidney disease?
- 1 April 1994
- journal article
- Published by Elsevier in Kidney International
- Vol. 45 (4) , 1153-1162
- https://doi.org/10.1038/ki.1994.153
Abstract
No abstract availableKeywords
This publication has 50 references indexed in Scilit:
- Unstable DNA may be responsible for the incomplete penetrance of the myotonic dystrophy phenotypeHuman Molecular Genetics, 1992
- Factors affecting the progression of renal disease in autosomal-dominant polycystic kidney diseaseKidney International, 1992
- Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndromePublished by Elsevier ,1991
- Patterns of inheritance of the symptoms of Huntington's disease suggestive of an effect of genomic imprinting.Journal of Medical Genetics, 1991
- Linkage Heterogeneity of Autosomal Dominant Polycystic Kidney DiseaseNew England Journal of Medicine, 1988
- Screening for polycystic kidney disease: importance of clinical presentation in the newborn.Archives of Disease in Childhood, 1987
- The enigma of the fragile X chromosomeTrends in Genetics, 1985
- Further segregation analysis of the fragile X syndrome with special reference to transmitting malesHuman Genetics, 1985
- Infantile presentation of adult-type polycystic kidney disease in a large kindredThe Journal of Pediatrics, 1975
- Congenital appearance of adult-type (autosomal dominant) polycystic kidney disease: Report of a caseThe Journal of Pediatrics, 1974