APA

Beygo J., Küchler A., Gillessen-Kaesbach G., Albrecht B., Eckle J., Eggermann T., Gellhaus A., Kanber D., Kordaß U., Lüdecke H., Purmann S., Rossier E., van de Nes J., van der Werf I. M., Wenzel M., Wieczorek D., Horsthemke B. & Buiting K. (20171212). New insights into the imprinted MEG8-DMR in 14q32 and clinical and molecular description of novel patients with Temple syndrome. : European journal of human genetics : EJHG.

Chicago

Beygo Jasmin, Küchler Alma, Gillessen-Kaesbach Gabriele, Albrecht Beate, Eckle Jonas, Eggermann Thomas, Gellhaus Alexandra, Kanber Deniz, Kordaß Ulrike, Lüdecke Hermann-Josef, Purmann Sabine, Rossier Eva, van de Nes Johannes, van der Werf Ilse M, Wenzel Maren, Wieczorek Dagmar, Horsthemke Bernhard and Buiting Karin. 20171212. New insights into the imprinted MEG8-DMR in 14q32 and clinical and molecular description of novel patients with Temple syndrome. : European journal of human genetics : EJHG.

Harvard

Beygo J., Küchler A., Gillessen-Kaesbach G., Albrecht B., Eckle J., Eggermann T., Gellhaus A., Kanber D., Kordaß U., Lüdecke H., Purmann S., Rossier E., van de Nes J., van der Werf I. M., Wenzel M., Wieczorek D., Horsthemke B. and Buiting K. (20171212). New insights into the imprinted MEG8-DMR in 14q32 and clinical and molecular description of novel patients with Temple syndrome. : European journal of human genetics : EJHG.

MLA

Beygo Jasmin, Küchler Alma, Gillessen-Kaesbach Gabriele, Albrecht Beate, Eckle Jonas, Eggermann Thomas, Gellhaus Alexandra, Kanber Deniz, Kordaß Ulrike, Lüdecke Hermann-Josef, Purmann Sabine, Rossier Eva, van de Nes Johannes, van der Werf Ilse M, Wenzel Maren, Wieczorek Dagmar, Horsthemke Bernhard and Buiting Karin. New insights into the imprinted MEG8-DMR in 14q32 and clinical and molecular description of novel patients with Temple syndrome. : European journal of human genetics : EJHG. 20171212.