APA

Peyrard-Janvid M., Leslie E. J., Kousa Y. A., Smith T. L., Dunnwald M., Magnusson M., Lentz B. A., Unneberg P., Fransson I., Koillinen H. K., Rautio J., Pegelow M., Karsten A., Basel-Vanagaite L., Gordon W., Andersen B., Svensson T., Murray J. C., Cornell R. A., Kere J. & Schutte B. C. (20140224). Dominant mutations in GRHL3 cause Van der Woude Syndrome and disrupt oral periderm development. : American journal of human genetics.

Chicago

Peyrard-Janvid Myriam, Leslie Elizabeth J, Kousa Youssef A, Smith Tiffany L, Dunnwald Martine, Magnusson Måns, Lentz Brian A, Unneberg Per, Fransson Ingegerd, Koillinen Hannele K, Rautio Jorma, Pegelow Marie, Karsten Agneta, Basel-Vanagaite Lina, Gordon William, Andersen Bogi, Svensson Thomas, Murray Jeffrey C, Cornell Robert A, Kere Juha and Schutte Brian C. 20140224. Dominant mutations in GRHL3 cause Van der Woude Syndrome and disrupt oral periderm development. : American journal of human genetics.

Harvard

Peyrard-Janvid M., Leslie E. J., Kousa Y. A., Smith T. L., Dunnwald M., Magnusson M., Lentz B. A., Unneberg P., Fransson I., Koillinen H. K., Rautio J., Pegelow M., Karsten A., Basel-Vanagaite L., Gordon W., Andersen B., Svensson T., Murray J. C., Cornell R. A., Kere J. and Schutte B. C. (20140224). Dominant mutations in GRHL3 cause Van der Woude Syndrome and disrupt oral periderm development. : American journal of human genetics.

MLA

Peyrard-Janvid Myriam, Leslie Elizabeth J, Kousa Youssef A, Smith Tiffany L, Dunnwald Martine, Magnusson Måns, Lentz Brian A, Unneberg Per, Fransson Ingegerd, Koillinen Hannele K, Rautio Jorma, Pegelow Marie, Karsten Agneta, Basel-Vanagaite Lina, Gordon William, Andersen Bogi, Svensson Thomas, Murray Jeffrey C, Cornell Robert A, Kere Juha and Schutte Brian C. Dominant mutations in GRHL3 cause Van der Woude Syndrome and disrupt oral periderm development. : American journal of human genetics. 20140224.