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	Positional cloning of a novel gene on chromosome 16q causing Bardet-Biedl syndrome (BBS2) [My Copy] Hum Mol Genet, Vol. 10, No. 8. (2001), pp. 865-74. by D. Y. Nishimura, C. C. Searby, R. Carmi, et al.K. Elbedour, L. V. Van Maldergem, A. B. Fulton, B. L. Lam, B. R. Powell, R. E. Swiderski, K. E. Bugge, N. B. Haider, A. E. Kwitek Black, L. Ying, D. M. Duhl, S. W. Gorman, E. Heon, A. Iannaccone, D. Bonneau, L. G. Biesecker, S. G. Jacobson, E. M. Stone, V. C. Sheffield posted to bbs cilia human bibtex-import by journal888 on 2005-04-23 06:42:28 as
	Bbs2-null mice have neurosensory deficits, a defect in social dominance, and retinopathy associated with mislocalization of rhodopsin [My Copy] Proc Natl Acad Sci U S A, Vol. 101, No. 47. (2004), pp. 16588-93. by D. Y. Nishimura, M. Fath, R. F. Mullins, et al.C. Searby, M. Andrews, R. Davis, J. L. Andorf, K. Mykytyn, R. E. Swiderski, B. Yang, R. Carmi, E. M. Stone, V. C. Sheffield posted to bbs cilia mouse bibtex-import by journal888 on 2005-04-23 06:42:28 as
	Identification of the gene (BBS1) most commonly involved in Bardet-Biedl syndrome, a complex human obesity syndrome [My Copy] Nat Genet, Vol. 31, No. 4. (2002), pp. 435-8. by K. Mykytyn, D. Y. Nishimura, C. C. Searby, et al.M. Shastri, H. J. Yen, J. S. Beck, T. Braun, L. M. Streb, A. S. Cornier, G. F. Cox, A. B. Fulton, R. Carmi, G. Luleci, S. C. Chandrasekharappa, F. S. Collins, S. G. Jacobson, J. R. Heckenlively, R. G. Weleber, E. M. Stone, V. C. Sheffield posted to bbs cilia human bibtex-import by journal888 on 2005-04-23 06:42:27 as
	Evaluation of complex inheritance involving the most common Bardet-Biedl syndrome locus (BBS1) [My Copy] Am J Hum Genet, Vol. 72, No. 2. (2003), pp. 429-37. by K. Mykytyn, D. Y. Nishimura, C. C. Searby, et al.G. Beck, K. Bugge, H. L. Haines, A. S. Cornier, G. F. Cox, A. B. Fulton, R. Carmi, A. Iannaccone, S. G. Jacobson, R. G. Weleber, A. F. Wright, R. Riise, R. C. Hennekam, G. Luleci, S. Berker Karauzum, L. G. Biesecker, E. M. Stone, V. C. Sheffield posted to bbs cilia human bibtex-import by journal888 on 2005-04-23 06:42:27 as
	Identification of the gene that, when mutated, causes the human obesity syndrome BBS4 [My Copy] Nat Genet, Vol. 28, No. 2. (2001), pp. 188-91. by K. Mykytyn, T. Braun, R. Carmi, et al.N. B. Haider, C. C. Searby, M. Shastri, G. Beck, A. F. Wright, A. Iannaccone, K. Elbedour, R. Riise, A. Baldi, A. Raas Rothschild, S. W. Gorman, D. M. Duhl, S. G. Jacobson, T. Casavant, E. M. Stone, V. C. Sheffield posted to bbs cilia human bibtex-import by journal888 on 2005-04-23 06:42:27 as

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