APA
Rauch A., Wieczorek D., Graf E., Wieland T., Endele S., Schwarzmayr T., Albrecht B., Bartholdi D., Beygo J., Di Donato N., Dufke A., Cremer K., Hempel M., Horn D., Hoyer J., Joset P., Röpke A., Moog U., Riess A., Thiel C. T., Tzschach A., Wiesener A., Wohlleber E., Zweier C., Ekici A. B., Zink A. M., Rump A., Meisinger C., Grallert H., Sticht H., Schenck A., Engels H., Rappold G., Schröck E., Wieacker P., Riess O., Meitinger T., Reis A. & Strom T. M. (20121203). Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study. : Lancet (London, England).
Chicago
Rauch Anita, Wieczorek Dagmar, Graf Elisabeth, Wieland Thomas, Endele Sabine, Schwarzmayr Thomas, Albrecht Beate, Bartholdi Deborah, Beygo Jasmin, Di Donato Nataliya, Dufke Andreas, Cremer Kirsten, Hempel Maja, Horn Denise, Hoyer Juliane, Joset Pascal, Röpke Albrecht, Moog Ute, Riess Angelika, Thiel Christian T, Tzschach Andreas, Wiesener Antje, Wohlleber Eva, Zweier Christiane, Ekici Arif B, Zink Alexander M, Rump Andreas, Meisinger Christa, Grallert Harald, Sticht Heinrich, Schenck Annette, Engels Hartmut, Rappold Gudrun, Schröck Evelin, Wieacker Peter, Riess Olaf, Meitinger Thomas, Reis André and Strom Tim M. 20121203. Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study. : Lancet (London, England).
Harvard
Rauch A., Wieczorek D., Graf E., Wieland T., Endele S., Schwarzmayr T., Albrecht B., Bartholdi D., Beygo J., Di Donato N., Dufke A., Cremer K., Hempel M., Horn D., Hoyer J., Joset P., Röpke A., Moog U., Riess A., Thiel C. T., Tzschach A., Wiesener A., Wohlleber E., Zweier C., Ekici A. B., Zink A. M., Rump A., Meisinger C., Grallert H., Sticht H., Schenck A., Engels H., Rappold G., Schröck E., Wieacker P., Riess O., Meitinger T., Reis A. and Strom T. M. (20121203). Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study. : Lancet (London, England).
MLA
Rauch Anita, Wieczorek Dagmar, Graf Elisabeth, Wieland Thomas, Endele Sabine, Schwarzmayr Thomas, Albrecht Beate, Bartholdi Deborah, Beygo Jasmin, Di Donato Nataliya, Dufke Andreas, Cremer Kirsten, Hempel Maja, Horn Denise, Hoyer Juliane, Joset Pascal, Röpke Albrecht, Moog Ute, Riess Angelika, Thiel Christian T, Tzschach Andreas, Wiesener Antje, Wohlleber Eva, Zweier Christiane, Ekici Arif B, Zink Alexander M, Rump Andreas, Meisinger Christa, Grallert Harald, Sticht Heinrich, Schenck Annette, Engels Hartmut, Rappold Gudrun, Schröck Evelin, Wieacker Peter, Riess Olaf, Meitinger Thomas, Reis André and Strom Tim M. Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study. : Lancet (London, England). 20121203.