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22. A kindred exhibiting cosegregation of an overlap connective tissue disorder and the chromosome 16 linked form of autosomal dominant polycystic kidney disease. Somlo S, Rutecki G, Giuffra LA, Reeders ST, Cugino A, Whittier FC. J Am Soc Nephrol; 1993 Dec; 4(6):1371-8. PubMed ID: 8130364 [Abstract] [Full Text] [Related]
26. Generation of a transcriptional map for a 700-kb region surrounding the polycystic kidney disease type 1 (PKD1) and tuberous sclerosis type 2 (TSC2) disease genes on human chromosome 16p3.3. Burn TC, Connors TD, Van Raay TJ, Dackowski WR, Millholland JM, Klinger KW, Landes GM. Genome Res; 1996 Jun; 6(6):525-37. PubMed ID: 8828041 [Abstract] [Full Text] [Related]
27. Human-mouse homologies in the region of the polycystic kidney disease gene (PKD1). Himmelbauer H, Pohlschmidt M, Snarey A, Germino GG, Weinstat-Saslow D, Somlo S, Reeders ST, Frischauf AM. Genomics; 1992 May; 13(1):35-8. PubMed ID: 1349580 [Abstract] [Full Text] [Related]
28. The diagnosis and prognosis of autosomal dominant polycystic kidney disease. Parfrey PS, Bear JC, Morgan J, Cramer BC, McManamon PJ, Gault MH, Churchill DN, Singh M, Hewitt R, Somlo S. N Engl J Med; 1990 Oct 18; 323(16):1085-90. PubMed ID: 2215575 [Abstract] [Full Text] [Related]
32. Two step procedure for early diagnosis of polycystic kidney disease with polymorphic DNA markers on both sides of the gene. Breuning MH, Snijdewint FG, Dauwerse JG, Saris JJ, Bakker E, Pearson PL, vanOmmen GJ. J Med Genet; 1990 Oct 18; 27(10):614-7. PubMed ID: 1978861 [Abstract] [Full Text] [Related]
39. Analysis of a large family with the second type of autosomal dominant polycystic kidney disease. Veldhuisen B, Breuning MH, Wesby-van Swaay E, Boersma J, Peters DJ. Nephrol Dial Transplant; 1996 Sep 18; 11 Suppl 6():13-7. PubMed ID: 9044321 [Abstract] [Full Text] [Related]