APA

Innes A. M., Boycott K. M., Puffenberger E. G., Redl D., MacDonald I. M., Chudley A. E., Beaulieu C., Perrier R., Gillan T., Wade A. & Parboosingh J. S. (20110217). A founder mutation in BBS2 is responsible for Bardet-Biedl syndrome in the Hutterite population: utility of SNP arrays in genetically heterogeneous disorders. : Clinical genetics.

Chicago

Innes A M, Boycott K M, Puffenberger E G, Redl D, MacDonald I M, Chudley A E, Beaulieu C, Perrier R, Gillan T, Wade A and Parboosingh J S. 20110217. A founder mutation in BBS2 is responsible for Bardet-Biedl syndrome in the Hutterite population: utility of SNP arrays in genetically heterogeneous disorders. : Clinical genetics.

Harvard

Innes A. M., Boycott K. M., Puffenberger E. G., Redl D., MacDonald I. M., Chudley A. E., Beaulieu C., Perrier R., Gillan T., Wade A. and Parboosingh J. S. (20110217). A founder mutation in BBS2 is responsible for Bardet-Biedl syndrome in the Hutterite population: utility of SNP arrays in genetically heterogeneous disorders. : Clinical genetics.

MLA

Innes A M, Boycott K M, Puffenberger E G, Redl D, MacDonald I M, Chudley A E, Beaulieu C, Perrier R, Gillan T, Wade A and Parboosingh J S. A founder mutation in BBS2 is responsible for Bardet-Biedl syndrome in the Hutterite population: utility of SNP arrays in genetically heterogeneous disorders. : Clinical genetics. 20110217.