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.