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11. Mutations in chaperonin-like BBS genes are a major contributor to disease development in a multiethnic Bardet-Biedl syndrome patient population. Billingsley G; Bin J; Fieggen KJ; Duncan JL; Gerth C; Ogata K; Wodak SS; Traboulsi EI; Fishman GA; Paterson A; Chitayat D; Knueppel T; Millán JM; Mitchell GA; Deveault C; Héon E J Med Genet; 2010 Jul; 47(7):453-63. PubMed ID: 20472660 [TBL] [Abstract][Full Text] [Related]
12. Clinical and molecular characterisation of Bardet-Biedl syndrome in consanguineous populations: the power of homozygosity mapping. Abu Safieh L; Aldahmesh MA; Shamseldin H; Hashem M; Shaheen R; Alkuraya H; Al Hazzaa SA; Al-Rajhi A; Alkuraya FS J Med Genet; 2010 Apr; 47(4):236-41. PubMed ID: 19858128 [TBL] [Abstract][Full Text] [Related]
13. Autozygosity mapping of Bardet-Biedl syndrome to 12q21.2 and confirmation of FLJ23560 as BBS10. White DR; Ganesh A; Nishimura D; Rattenberry E; Ahmed S; Smith UM; Pasha S; Raeburn S; Trembath RC; Rajab A; Macdonald F; Banin E; Stone EM; Johnson CA; Sheffield VC; Maher ER Eur J Hum Genet; 2007 Feb; 15(2):173-8. PubMed ID: 17106446 [TBL] [Abstract][Full Text] [Related]
14. Linkage mapping in 29 Bardet-Biedl syndrome families confirms loci in chromosomal regions 11q13, 15q22.3-q23, and 16q21. Bruford EA; Riise R; Teague PW; Porter K; Thomson KL; Moore AT; Jay M; Warburg M; Schinzel A; Tommerup N; Tornqvist K; Rosenberg T; Patton M; Mansfield DC; Wright AF Genomics; 1997 Apr; 41(1):93-9. PubMed ID: 9126487 [TBL] [Abstract][Full Text] [Related]
15. Bardet-Biedl syndrome is linked to DNA markers on chromosome 11q and is genetically heterogeneous. Leppert M; Baird L; Anderson KL; Otterud B; Lupski JR; Lewis RA Nat Genet; 1994 May; 7(1):108-12. PubMed ID: 8075632 [TBL] [Abstract][Full Text] [Related]
16. Novel homozygous mutations in the genes ARL6 and BBS10 underlying Bardet-Biedl syndrome. Khan S; Ullah I; Irfanullah ; Touseef M; Basit S; Khan MN; Ahmad W Gene; 2013 Feb; 515(1):84-8. PubMed ID: 23219996 [TBL] [Abstract][Full Text] [Related]
17. Genetic heterogeneity of Bardet-Biedl syndrome in a distinct Canadian population: evidence for a fifth locus. Woods MO; Young TL; Parfrey PS; Hefferton D; Green JS; Davidson WS Genomics; 1999 Jan; 55(1):2-9. PubMed ID: 9888993 [TBL] [Abstract][Full Text] [Related]
18. Basal body dysfunction is a likely cause of pleiotropic Bardet-Biedl syndrome. Ansley SJ; Badano JL; Blacque OE; Hill J; Hoskins BE; Leitch CC; Kim JC; Ross AJ; Eichers ER; Teslovich TM; Mah AK; Johnsen RC; Cavender JC; Lewis RA; Leroux MR; Beales PL; Katsanis N Nature; 2003 Oct; 425(6958):628-33. PubMed ID: 14520415 [TBL] [Abstract][Full Text] [Related]
19. Use of isolated populations in the study of a human obesity syndrome, the Bardet-Biedl syndrome. Sheffield VC Pediatr Res; 2004 Jun; 55(6):908-11. PubMed ID: 15155861 [TBL] [Abstract][Full Text] [Related]
20. A novel H395R mutation in MKKS/BBS6 causes retinitis pigmentosa and polydactyly without other findings of Bardet-Biedl or McKusick-Kaufman syndrome. Hulleman JD; Nguyen A; Ramprasad VL; Murugan S; Gupta R; Mahindrakar A; Angara R; Sankurathri C; Mootha VV Mol Vis; 2016; 22():73-81. PubMed ID: 26900326 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]