New insights into the imprinted MEG8-DMR in 14q32 and clinical and molecular description of novel patients with Temple syndrome

Beygo, Jasmin; Kuechler, Alma; Gillessen-Kaesbach, Gabriele; Albrecht, Beate; Eckle, Jonas; Eggermann, Thomas; Gellhaus, Alexandra; Kanber, Deniz; Kordass, Ulrike; Luedecke, Hermann-Josef; Purmann, Sabine; Rossier, Eva; van de Nes, Johannes; van der Werf, Ilse M.; Wenzel, Maren; Wieczorek, Dagmar; Horsthemke, Bernhard; Buiting, Karin

New insights into the imprinted MEG8-DMR in 14q32 and clinical and molecular description of novel patients with Temple syndrome

Autor(en):

Beygo, Jasmin; Kuechler, Alma; Gillessen-Kaesbach, Gabriele; Albrecht, Beate; Eckle, Jonas; Eggermann, Thomas; Gellhaus, Alexandra; Kanber, Deniz; Kordass, Ulrike; Luedecke, Hermann-Josef; Purmann, Sabine; Rossier, Eva; van de Nes, Johannes; van der Werf, Ilse M.; Wenzel, Maren; Wieczorek, Dagmar; Horsthemke, Bernhard; Buiting, Karin

Tübinger Autor(en):

Rossier, Eva

Erschienen in:

European Journal of Human Genetics (2017), Bd. 25, H. 8, S. 935-945

Verlagsangabe:

Nature Publishing Group

Sprache:

Englisch

Referenz zum Volltext:

http://dx.doi.org/10.1038/ejhg.2017.91

ISSN:

1476-5438