APA
Koenig M., Beggs A. H., Moyer M., Scherpf S., Heindrich K., Bettecken T., Meng G., Müller C. R., Lindlöf M., Kaariainen H., de la Chapellet A., Kiuru A., Savontaus M. L., Gilgenkrantz H., Récan D., Chelly J., Kaplan J. C., Covone A. E., Archidiacono N., Romeo G., Liechti-Gailati S., Schneider V., Braga S., Moser H., Darras B. T., Murphy P., Francke U., Chen J. D., Morgan G., Denton M., Greenberg C. R., Wrogemann K., Blonden L. A., van Paassen M. B., van Ommen G. J. & Kunkel L. M. (19910918). The molecular basis for Duchenne versus Becker muscular dystrophy: correlation of severity with type of deletion. : American journal of human genetics.
Chicago
Koenig M, Beggs A H, Moyer M, Scherpf S, Heindrich K, Bettecken T, Meng G, Müller C R, Lindlöf M, Kaariainen H, de la Chapellet A, Kiuru A, Savontaus M L, Gilgenkrantz H, Récan D, Chelly J, Kaplan J C, Covone A E, Archidiacono N, Romeo G, Liechti-Gailati S, Schneider V, Braga S, Moser H, Darras B T, Murphy P, Francke U, Chen J D, Morgan G, Denton M, Greenberg C R, Wrogemann K, Blonden L A, van Paassen M B, van Ommen G J and Kunkel L M. 19910918. The molecular basis for Duchenne versus Becker muscular dystrophy: correlation of severity with type of deletion. : American journal of human genetics.
Harvard
Koenig M., Beggs A. H., Moyer M., Scherpf S., Heindrich K., Bettecken T., Meng G., Müller C. R., Lindlöf M., Kaariainen H., de la Chapellet A., Kiuru A., Savontaus M. L., Gilgenkrantz H., Récan D., Chelly J., Kaplan J. C., Covone A. E., Archidiacono N., Romeo G., Liechti-Gailati S., Schneider V., Braga S., Moser H., Darras B. T., Murphy P., Francke U., Chen J. D., Morgan G., Denton M., Greenberg C. R., Wrogemann K., Blonden L. A., van Paassen M. B., van Ommen G. J. and Kunkel L. M. (19910918). The molecular basis for Duchenne versus Becker muscular dystrophy: correlation of severity with type of deletion. : American journal of human genetics.
MLA
Koenig M, Beggs A H, Moyer M, Scherpf S, Heindrich K, Bettecken T, Meng G, Müller C R, Lindlöf M, Kaariainen H, de la Chapellet A, Kiuru A, Savontaus M L, Gilgenkrantz H, Récan D, Chelly J, Kaplan J C, Covone A E, Archidiacono N, Romeo G, Liechti-Gailati S, Schneider V, Braga S, Moser H, Darras B T, Murphy P, Francke U, Chen J D, Morgan G, Denton M, Greenberg C R, Wrogemann K, Blonden L A, van Paassen M B, van Ommen G J and Kunkel L M. The molecular basis for Duchenne versus Becker muscular dystrophy: correlation of severity with type of deletion. : American journal of human genetics. 19910918.