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Hum Genet ; 91(6): 609-13, 1993 Jul.
Article in English | MEDLINE | ID: mdl-8340115

ABSTRACT

We have mainly used 3 highly polymorphic DNA markers, 3'HVR (D16S85), 16AC2.5 (D16S291) and SM7 (D16S283), flanking the PKD1 region on chromosome 16p13.3 to establish linkage status in seven Icelandic families with autosomal dominant polycystic kidney disease (ADPKD). In four families, the disease locus is in the PKD1 region, and three families are "unlinked" to chromosome 16p13.3. In one of the "unlinked" families, the disease locus is excluded from a part of the long arm of chromosome 2, and we support a theory of more than 2 loci being responsible for ADPKD. Our data confirm the location of the locus YNH24 (D2S44) to chromosome 2q13-q24.


Subject(s)
Chromosomes, Human, Pair 16 , Chromosomes, Human, Pair 2 , Polycystic Kidney, Autosomal Dominant/genetics , Adult , Genetic Markers , Humans , Iceland , Polymerase Chain Reaction
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