Clinical and genetic epidemiology of inherited renal disease in Newfoundland Patrick S. Parfrey, William S. Davidson, Jane S. Green Kidney International Volume 61, Issue 6, Pages 1925-1934 (June 2002) DOI: 10.1046/j.1523-1755.2002.00305.x Copyright © 2002 International Society of Nephrology Terms and Conditions
Figure 1 Geographic distribution of PKD1 and PKD2 families in Newfoundland. Mutation status, inferred by haplotype analysis, is noted by bracketed letter. The four families with the identical haplotype around the PKD1, transmitted with PKD, locus are labeled PKD1 (A). Kidney International 2002 61, 1925-1934DOI: (10.1046/j.1523-1755.2002.00305.x) Copyright © 2002 International Society of Nephrology Terms and Conditions
Figure 2 Geographic distribution of Bardet-Biedl syndrome (BBS) in Newfoundland families by identification numbers (B1–B19) and by genotype (BBS1-6). Kidney International 2002 61, 1925-1934DOI: (10.1046/j.1523-1755.2002.00305.x) Copyright © 2002 International Society of Nephrology Terms and Conditions
Figure 3 Age of diagnosis of blindness (▪), hypertension (□), and renal impairment (▴) in Bardet-Biedl syndrome patients. Kidney International 2002 61, 1925-1934DOI: (10.1046/j.1523-1755.2002.00305.x) Copyright © 2002 International Society of Nephrology Terms and Conditions