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Nature Genetics|December 1, 1994
Deletion of the TSC2 and PKD1 genes associated with severe infantile polycystic kidney disease--a contiguous gene syndromeP T Brook-Carter, B Peral, C J Ward, et al.Lancet (London, England)|October 7, 1989
Detection of breakpoints in submicroscopic chromosomal translocation, illustrating an important mechanism for genetic diseaseJ Lamb, A O Wilkie, P C Harris, et al.Proceedings of the National Academy of Sciences of the United States of America|January 1, 1992
Construction of a map of chromosome 16 by using radiation hybridsI Ceccherini, G Romeo, S Lawrence, et al.American Journal of Human Genetics|August 1, 1994
Linkage disequilibrium in the region of the autosomal dominant polycystic kidney disease gene (PKD1)A Snarey, S Thomas, M C Schneider, et al.Cell|February 8, 1991
Stable length polymorphism of up to 260 kb at the tip of the short arm of human chromosome 16A O Wilkie, D R Higgs, K A Rack, et al.Proceedings of the National Academy of Sciences of the United States of America|March 17, 2001
Polycystin-2, the protein mutated in autosomal dominant polycystic kidney disease (ADPKD), is a Ca2+-permeable nonselective cation channelS González-Perrett, K Kim, C Ibarra, et al.Genomics|June 1, 1991
A refined physical map of the long arm of human chromosome 16L Z Chen, P C Harris, S Apostolou, et al.European Journal of Clinical Investigation|February 9, 2008
Co-inheritance of a PKD1 mutation and homozygous PKD2 variant: a potential modifier in autosomal dominant polycystic kidney diseaseG V Z Dedoussis, Y Luo, P Starremans, et al.American Journal of Human Genetics|November 15, 2000
Identification of a locus for autosomal dominant polycystic liver disease, on chromosome 19p13.2-13.1D M Reynolds, C T Falk, A Li, et al.Proceedings of the National Academy of Sciences of the United States of America|January 7, 1997
Cloning and characterization of a functional human homolog of Escherichia coli endonuclease IIIR Aspinwall, D G Rothwell, T Roldan-Arjona, et al.Pageof 16