APA
Bauwens M., Garanto A., Sangermano R., Naessens S., Weisschuh N., De Zaeytijd J., Khan M., Sadler F., Balikova I., Van Cauwenbergh C., Rosseel T., Bauwens J., De Leeneer K., De Jaegere S., Van Laethem T., De Vries M., Carss K., Arno G., Fakin A., Webster A. R., de Ravel de l'Argentière T. J. L., Sznajer Y., Vuylsteke M., Kohl S., Wissinger B., Cherry T., Collin R. W. J., Cremers F. P. M., Leroy B. P. & De Baere E. (20200206). ABCA4-associated disease as a model for missing heritability in autosomal recessive disorders: novel noncoding splice, cis-regulatory, structural, and recurrent hypomorphic variants. : Genetics in medicine : official journal of the American College of Medical Genetics.
Chicago
Bauwens Miriam, Garanto Alejandro, Sangermano Riccardo, Naessens Sarah, Weisschuh Nicole, De Zaeytijd Julie, Khan Mubeen, Sadler Françoise, Balikova Irina, Van Cauwenbergh Caroline, Rosseel Toon, Bauwens Jim, De Leeneer Kim, De Jaegere Sarah, Van Laethem Thalia, De Vries Meindert, Carss Keren, Arno Gavin, Fakin Ana, Webster Andrew R, de Ravel de l'Argentière Thomy J L, Sznajer Yves, Vuylsteke Marnik, Kohl Susanne, Wissinger Bernd, Cherry Timothy, Collin Rob W J, Cremers Frans P M, Leroy Bart P and De Baere Elfride. 20200206. ABCA4-associated disease as a model for missing heritability in autosomal recessive disorders: novel noncoding splice, cis-regulatory, structural, and recurrent hypomorphic variants. : Genetics in medicine : official journal of the American College of Medical Genetics.
Harvard
Bauwens M., Garanto A., Sangermano R., Naessens S., Weisschuh N., De Zaeytijd J., Khan M., Sadler F., Balikova I., Van Cauwenbergh C., Rosseel T., Bauwens J., De Leeneer K., De Jaegere S., Van Laethem T., De Vries M., Carss K., Arno G., Fakin A., Webster A. R., de Ravel de l'Argentière T. J. L., Sznajer Y., Vuylsteke M., Kohl S., Wissinger B., Cherry T., Collin R. W. J., Cremers F. P. M., Leroy B. P. and De Baere E. (20200206). ABCA4-associated disease as a model for missing heritability in autosomal recessive disorders: novel noncoding splice, cis-regulatory, structural, and recurrent hypomorphic variants. : Genetics in medicine : official journal of the American College of Medical Genetics.
MLA
Bauwens Miriam, Garanto Alejandro, Sangermano Riccardo, Naessens Sarah, Weisschuh Nicole, De Zaeytijd Julie, Khan Mubeen, Sadler Françoise, Balikova Irina, Van Cauwenbergh Caroline, Rosseel Toon, Bauwens Jim, De Leeneer Kim, De Jaegere Sarah, Van Laethem Thalia, De Vries Meindert, Carss Keren, Arno Gavin, Fakin Ana, Webster Andrew R, de Ravel de l'Argentière Thomy J L, Sznajer Yves, Vuylsteke Marnik, Kohl Susanne, Wissinger Bernd, Cherry Timothy, Collin Rob W J, Cremers Frans P M, Leroy Bart P and De Baere Elfride. ABCA4-associated disease as a model for missing heritability in autosomal recessive disorders: novel noncoding splice, cis-regulatory, structural, and recurrent hypomorphic variants. : Genetics in medicine : official journal of the American College of Medical Genetics. 20200206.