The application of molecular biology to the prenatal diagnosis of renal disease
- PMID: 3153039
- DOI: 10.1007/BF00858691
The application of molecular biology to the prenatal diagnosis of renal disease
Abstract
The rapid development of new techniques in molecular biology is leading to identification of the genes responsible for a wide variety of diseases. Several renal conditions are caused by gene defects and are amenable to this approach. The process of gene mapping is discussed and the current position regarding prenatal diagnosis and carrier testing for genetic renal disease is reviewed.
Similar articles
-
[Inherited renal diseases and prenatal diagnosis].Arch Pediatr. 2006 Jun;13(6):727-9. doi: 10.1016/j.arcped.2006.03.064. Epub 2006 May 11. Arch Pediatr. 2006. PMID: 16697565 French. No abstract available.
-
[Hereditary kidney diseases in children (a review of the literature)].Vopr Okhr Materin Det. 1973 Mar;18(3):36-40. Vopr Okhr Materin Det. 1973. PMID: 4585577 Review. Russian. No abstract available.
-
Prenatal diagnosis of adult polycystic kidney disease with DNA markers on chromosome 16 and the genetic heterogeneity problem.Prenat Diagn. 1989 Nov;9(11):759-67. doi: 10.1002/pd.1970091104. Prenat Diagn. 1989. PMID: 2616535
-
Current concepts in sonographic diagnosis of fetal renal disease.Radiographics. 1988 Jan;8(1):119-32. doi: 10.1148/radiographics.8.1.3281192. Radiographics. 1988. PMID: 3281192
-
[Hereditary renal diseases and their genetic diagnosis].Duodecim. 1995;111(15):1398-400. Duodecim. 1995. PMID: 9244694 Review. Finnish. No abstract available.
References
Publication types
MeSH terms
Substances
LinkOut - more resources
Medical