Mutations in chaperonin-like BBS genes are a major contributor to disease development in a multiethnic Bardet-Biedl syndrome patient population - Billingsley, Gail; Bin, Jenea; Fieggen, Karen J.; Duncan, Jacque L.; Gerth, Christina; Ogata, Koji; Wodak, Shoshana S.; Traboulsi, Elias I.; Fishman, Gerald A.; Paterson, Andrew; Chitayat, David; Knüppel, Tanja; et al. (Journal of medical genetics, 2010)
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