APA

Gordon C. T., Xue S., Yigit G., Filali H., Chen K., Rosin N., Yoshiura K., Oufadem M., Beck T. J., McGowan R., Magee A. C., Altmüller J., Dion C., Thiele H., Gurzau A. D., Nürnberg P., Meschede D., Mühlbauer W., Okamoto N., Varghese V., Irving R., Sigaudy S., Williams D., Ahmed S. F., Bonnard C., Kong M. K., Ratbi I., Fejjal N., Fikri M., Elalaoui S. C., Reigstad H., Bole-Feysot C., Nitschké P., Ragge N., Lévy N., Tunçbilek G., Teo A. S. M., Cunningham M. L., Sefiani A., Kayserili H., Murphy J. M., Chatdokmaiprai C., Hillmer A. M., Wattanasirichaigoon D., Lyonnet S., Magdinier F., Javed A., Blewitt M. E., Amiel J., Wollnik B. & Reversade B. (20170905). De novo mutations in SMCHD1 cause Bosma arhinia microphthalmia syndrome and abrogate nasal development. : Nature genetics.

Chicago

Gordon Christopher T, Xue Shifeng, Yigit Gökhan, Filali Hicham, Chen Kelan, Rosin Nadine, Yoshiura Koh-Ichiro, Oufadem Myriam, Beck Tamara J, McGowan Ruth, Magee Alex C, Altmüller Janine, Dion Camille, Thiele Holger, Gurzau Alexandra D, Nürnberg Peter, Meschede Dieter, Mühlbauer Wolfgang, Okamoto Nobuhiko, Varghese Vinod, Irving Rachel, Sigaudy Sabine, Williams Denise, Ahmed S Faisal, Bonnard Carine, Kong Mung Kei, Ratbi Ilham, Fejjal Nawfal, Fikri Meriem, Elalaoui Siham Chafai, Reigstad Hallvard, Bole-Feysot Christine, Nitschké Patrick, Ragge Nicola, Lévy Nicolas, Tunçbilek Gökhan, Teo Audrey S M, Cunningham Michael L, Sefiani Abdelaziz, Kayserili Hülya, Murphy James M, Chatdokmaiprai Chalermpong, Hillmer Axel M, Wattanasirichaigoon Duangrurdee, Lyonnet Stanislas, Magdinier Frédérique, Javed Asif, Blewitt Marnie E, Amiel Jeanne, Wollnik Bernd and Reversade Bruno. 20170905. De novo mutations in SMCHD1 cause Bosma arhinia microphthalmia syndrome and abrogate nasal development. : Nature genetics.

Harvard

Gordon C. T., Xue S., Yigit G., Filali H., Chen K., Rosin N., Yoshiura K., Oufadem M., Beck T. J., McGowan R., Magee A. C., Altmüller J., Dion C., Thiele H., Gurzau A. D., Nürnberg P., Meschede D., Mühlbauer W., Okamoto N., Varghese V., Irving R., Sigaudy S., Williams D., Ahmed S. F., Bonnard C., Kong M. K., Ratbi I., Fejjal N., Fikri M., Elalaoui S. C., Reigstad H., Bole-Feysot C., Nitschké P., Ragge N., Lévy N., Tunçbilek G., Teo A. S. M., Cunningham M. L., Sefiani A., Kayserili H., Murphy J. M., Chatdokmaiprai C., Hillmer A. M., Wattanasirichaigoon D., Lyonnet S., Magdinier F., Javed A., Blewitt M. E., Amiel J., Wollnik B. and Reversade B. (20170905). De novo mutations in SMCHD1 cause Bosma arhinia microphthalmia syndrome and abrogate nasal development. : Nature genetics.

MLA

Gordon Christopher T, Xue Shifeng, Yigit Gökhan, Filali Hicham, Chen Kelan, Rosin Nadine, Yoshiura Koh-Ichiro, Oufadem Myriam, Beck Tamara J, McGowan Ruth, Magee Alex C, Altmüller Janine, Dion Camille, Thiele Holger, Gurzau Alexandra D, Nürnberg Peter, Meschede Dieter, Mühlbauer Wolfgang, Okamoto Nobuhiko, Varghese Vinod, Irving Rachel, Sigaudy Sabine, Williams Denise, Ahmed S Faisal, Bonnard Carine, Kong Mung Kei, Ratbi Ilham, Fejjal Nawfal, Fikri Meriem, Elalaoui Siham Chafai, Reigstad Hallvard, Bole-Feysot Christine, Nitschké Patrick, Ragge Nicola, Lévy Nicolas, Tunçbilek Gökhan, Teo Audrey S M, Cunningham Michael L, Sefiani Abdelaziz, Kayserili Hülya, Murphy James M, Chatdokmaiprai Chalermpong, Hillmer Axel M, Wattanasirichaigoon Duangrurdee, Lyonnet Stanislas, Magdinier Frédérique, Javed Asif, Blewitt Marnie E, Amiel Jeanne, Wollnik Bernd and Reversade Bruno. De novo mutations in SMCHD1 cause Bosma arhinia microphthalmia syndrome and abrogate nasal development. : Nature genetics. 20170905.