Two step procedure for early diagnosis of polycystic kidney disease with polymorphic DNA markers on both sides of the gene.

Author:

Breuning M H,Snijdewint F G,Dauwerse J G,Saris J J,Bakker E,Pearson P L,vanOmmen G J

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference22 articles.

1. Age at clinical onset and at ultrasonographic detection of adult polycystic kidney techniques, the polymorphisms can be visualised rapidly without using radioactive label. Using disease-data for genetic counseling;Bear, J.C.; McManamon, P.; Morgan, J.;AmJ Med Genet,1984

2. A new hypervariable marker for the denaturing gradient gel electrophoresis (DGGE),22 we human alpha globin gene cluster;Am J Hum Genet; 43: have detected polymorphisms in the sequence recognised by 26-6.3 We are now designing a set of PCR,1988

3. Isolation and mapping identification of haplotypes within families. If this strategy bears fruit, the diagnosis of polycystic kidney of a polymorphic DNA sequence (pCMM65) on chromosome;Nakamura, Y.; Martin, C.; Krapcho, K.;Nucleic Acids Res,1988

4. DNA probe analysis disease using linked DNA markers will be much for carrier detection and prenatal diagnosis of Duchenne improved. The search for the PKD1 gene is now drawing to a muscular dystrophy: a standard diagnostic procedure;Bakker, E.; Bonten, E.J.; de Lange, L.F.;J Med Genet,1986

5. Topography close. Flanking markers are available, and the long range restriction map of the region is almost complete of the Duchenne muscular dystrophy (DMD) gene: FIGE and cDNA analysis of;IT, Den Dunnen; PM, Grootscholten; E, Bakker;Am J Hum Genet; cases reveals 115 deletions and 13 duplications,1989

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