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Citation: Pl. Beales et al., Genetic and mutational analyses of a large multiethnic Bardet-Biedl cohortreveal a minor involvement of BBS6 and delineate the critical intervals ofother loci, AM J HU GEN, 68(3), 2001, pp. 606-616

Authors: Katsanis, N Beales, PL Woods, MO Lewis, RA Green, JS Parfrey, PS Ansley, SJ Davidson, WS Lupski, JR

Citation: N. Katsanis et al., Mutations in MKKS cause obesity, retinal dystrophy and renal malformationsassociated with Bardet-Biedl syndrome, NAT GENET, 26(1), 2000, pp. 67-70

Authors: Woods, MO Young, TL Parfrey, PS Hefferton, D Green, JS Davidson, WS

Citation: Mo. Woods et al., Genetic heterogeneity of Bardet-Biedl syndrome in a distinct Canadian population: Evidence for a fifth locus, GENOMICS, 55(1), 1999, pp. 2-9

Authors: Young, TL Woods, MO Parfrey, PS Green, JS Hefferton, D Davidson, WS

Citation: Tl. Young et al., A founder effect in the Newfoundland population reduces the Bardet-Biedl syndrome I (BBS1) interval to 1 cM, AM J HU GEN, 65(6), 1999, pp. 1680-1687

Authors: Young, TL Penney, L Woods, MO Parfrey, PS Green, JS Hefferton, D Davidson, WS

Citation: Tl. Young et al., A fifth locus for Bardet-Biedl syndrome maps to chromosome 2q31, AM J HU GEN, 64(3), 1999, pp. 900-904