APA
Harris E., Topf A., Barresi R., Hudson J., Powell H., Tellez J., Hicks D., Porter A., Bertoli M., Evangelista T., Marini-Betollo C., Magnússon Ó., Lek M., MacArthur D., Bushby K., Lochmüller H. & Straub V. (20180521). Exome sequences versus sequential gene testing in the UK highly specialised Service for Limb Girdle Muscular Dystrophy. : Orphanet journal of rare diseases.
Chicago
Harris Elizabeth, Topf Ana, Barresi Rita, Hudson Judith, Powell Helen, Tellez James, Hicks Debbie, Porter Anna, Bertoli Marta, Evangelista Teresinha, Marini-Betollo Chiara, Magnússon Ólafur, Lek Monkol, MacArthur Daniel, Bushby Kate, Lochmüller Hanns and Straub Volker. 20180521. Exome sequences versus sequential gene testing in the UK highly specialised Service for Limb Girdle Muscular Dystrophy. : Orphanet journal of rare diseases.
Harvard
Harris E., Topf A., Barresi R., Hudson J., Powell H., Tellez J., Hicks D., Porter A., Bertoli M., Evangelista T., Marini-Betollo C., Magnússon Ó., Lek M., MacArthur D., Bushby K., Lochmüller H. and Straub V. (20180521). Exome sequences versus sequential gene testing in the UK highly specialised Service for Limb Girdle Muscular Dystrophy. : Orphanet journal of rare diseases.
MLA
Harris Elizabeth, Topf Ana, Barresi Rita, Hudson Judith, Powell Helen, Tellez James, Hicks Debbie, Porter Anna, Bertoli Marta, Evangelista Teresinha, Marini-Betollo Chiara, Magnússon Ólafur, Lek Monkol, MacArthur Daniel, Bushby Kate, Lochmüller Hanns and Straub Volker. Exome sequences versus sequential gene testing in the UK highly specialised Service for Limb Girdle Muscular Dystrophy. : Orphanet journal of rare diseases. 20180521.