Exploring the phenotypical spectrum of BRD4 defects

Hauer N, Vogl C, Popp B, Buettner C, Uebe S, Sticht H, Ekici AB, Klinger P, Kraus C, Krumbiegel M, Wiesener A, Dörr HG, Wiesmann da Silva Reis A, Thiel C (2019)

Publication Type: Conference contribution

Publication year: 2019

Journal

European Journal of Human Genetics Nature Publishing Group: Open Access Hybrid Model Option B

Publisher: NATURE PUBLISHING GROUP

City/Town: LONDON

Pages Range: 1380-1380

Conference Proceedings Title: EUROPEAN JOURNAL OF HUMAN GENETICS

Event location: Gothenburg, SWEDEN

Authors with CRIS profile

Nadine Hauer Lehrstuhl für Humangenetik Bernt Popp Institute of Human Genetics Heinrich Sticht Professur für Bioinformatik Arif Bülent Ekici Institute of Human Genetics Patricia Klinger Lehrstuhl für Funktionelle und Klinische Anatomie Helmuth-Günther Dörr Medizinische Fakultät André Wiesmann da Silva Reis Lehrstuhl für Humangenetik Christian Thiel Medizinische Fakultät

How to cite

APA:

Hauer, N., Vogl, C., Popp, B., Buettner, C., Uebe, S., Sticht, H.,... Thiel, C. (2019). Exploring the phenotypical spectrum of BRD4 defects. In EUROPEAN JOURNAL OF HUMAN GENETICS (pp. 1380-1380). Gothenburg, SWEDEN: LONDON: NATURE PUBLISHING GROUP.

MLA:

Hauer, Nadine, et al. "Exploring the phenotypical spectrum of BRD4 defects." Proceedings of the 52nd Conference of the European-Society-of-Human-Genetics (ESHG), Gothenburg, SWEDEN LONDON: NATURE PUBLISHING GROUP, 2019. 1380-1380.

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