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	1.	A computational/functional genomics approach for the enrichment of the retinal transcriptome and the identification of positional candidate retinopathy genes. [electronic resource] by Katsanis, Nicholas Worley, Kim C Gonzalez, Guillermo Ansley, Stephen J Lupski, James R Producer: 20021209 In: Proceedings of the National Academy of Sciences of the United States of America vol. 99 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Identification of a novel Bardet-Biedl syndrome protein, BBS7, that shares structural features with BBS1 and BBS2. [electronic resource] by Badano, José L Ansley, Stephen J Leitch, Carmen C Lewis, Richard Alan Lupski, James R Katsanis, Nicholas Producer: 20030424 In: American journal of human genetics vol. 72 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	BBS4 is a minor contributor to Bardet-Biedl syndrome and may also participate in triallelic inheritance. [electronic resource] by Katsanis, Nicholas Eichers, Erica R Ansley, Stephen J Lewis, Richard Alan Kayserili, Hülya Hoskins, Bethan E Scambler, Peter J Beales, Philip L Lupski, James R Producer: 20020726 In: American journal of human genetics vol. 71 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Dissection of epistasis in oligogenic Bardet-Biedl syndrome. [electronic resource] by Badano, Jose L Leitch, Carmen C Ansley, Stephen J May-Simera, Helen Lawson, Shaneka Lewis, Richard Alan Beales, Philip L Dietz, Harry C Fisher, Shannon Katsanis, Nicholas Producer: 20060214 In: Nature vol. 439 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Heterozygous mutations in BBS1, BBS2 and BBS6 have a potential epistatic effect on Bardet-Biedl patients with two mutations at a second BBS locus. [electronic resource] by Badano, Jose L Kim, Jun Chul Hoskins, Bethan E Lewis, Richard Alan Ansley, Stephen J Cutler, David J Castellan, Claudio Beales, Philip L Leroux, Michel R Katsanis, Nicholas Producer: 20031003 In: Human molecular genetics vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Genetic interaction of BBS1 mutations with alleles at other BBS loci can result in non-Mendelian Bardet-Biedl syndrome. [electronic resource] by Beales, Philip L Badano, Jose L Ross, Alison J Ansley, Stephen J Hoskins, Bethan E Kirsten, Brigitta Mein, Charles A Froguel, Philippe Scambler, Peter J Lewis, Richard Alan Lupski, James R Katsanis, Nicholas Producer: 20030701 In: American journal of human genetics vol. 72 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	The Bardet-Biedl protein BBS4 targets cargo to the pericentriolar region and is required for microtubule anchoring and cell cycle progression. [electronic resource] by Kim, Jun Chul Badano, Jose L Sibold, Sonja Esmail, Muneer A Hill, Josephine Hoskins, Bethan E Leitch, Carmen C Venner, Kerrie Ansley, Stephen J Ross, Alison J Leroux, Michel R Katsanis, Nicholas Beales, Philip L Producer: 20040525 In: Nature genetics vol. 36 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Basal body dysfunction is a likely cause of pleiotropic Bardet-Biedl syndrome. [electronic resource] by Ansley, Stephen J Badano, Jose L Blacque, Oliver E Hill, Josephine Hoskins, Bethan E Leitch, Carmen C Kim, Jun Chul Ross, Alison J Eichers, Erica R Teslovich, Tanya M Mah, Allan K Johnsen, Robert C Cavender, John C Lewis, Richard Alan Leroux, Michel R Beales, Philip L Katsanis, Nicholas Producer: 20031104 In: Nature vol. 425 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Loss of C. elegans BBS-7 and BBS-8 protein function results in cilia defects and compromised intraflagellar transport. [electronic resource] by Blacque, Oliver E Reardon, Michael J Li, Chunmei McCarthy, Jonathan Mahjoub, Moe R Ansley, Stephen J Badano, Jose L Mah, Allan K Beales, Philip L Davidson, William S Johnsen, Robert C Audeh, Mark Plasterk, Ronald H A Baillie, David L Katsanis, Nicholas Quarmby, Lynne M Wicks, Stephen R Leroux, Michel R Producer: 20040812 In: Genes & development vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Mutations in a member of the Ras superfamily of small GTP-binding proteins causes Bardet-Biedl syndrome. [electronic resource] by Fan, Yanli Esmail, Muneer A Ansley, Stephen J Blacque, Oliver E Boroevich, Keith Ross, Alison J Moore, Susan J Badano, Jose L May-Simera, Helen Compton, Deanna S Green, Jane S Lewis, Richard Alan van Haelst, Mieke M Parfrey, Patrick S Baillie, David L Beales, Philip L Katsanis, Nicholas Davidson, William S Leroux, Michel R Producer: 20041004 In: Nature genetics vol. 36 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)