Whole-exome sequencing identifies novel causative variants and expands the phenotypic spectrum of PLK4-related primary microcephaly

Boonsawat P, Asadollahi R, Niedrist D, Joset P, Wisser J, Budka H, Bode PK, Sticht H, Steindl K, Rauch A (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: 28-29

Conference Proceedings Title: EUROPEAN JOURNAL OF HUMAN GENETICS

Event location: Milan, ITALY

Authors with CRIS profile

Heinrich Sticht Professur für Bioinformatik

Involved external institutions

University of Zurich / Universität Zürich (UZH) CH Switzerland (CH) University of Newcastle (UoN) AU Australia (AU)

How to cite

APA:

Boonsawat, P., Asadollahi, R., Niedrist, D., Joset, P., Wisser, J., Budka, H.,... Rauch, A. (2019). Whole-exome sequencing identifies novel causative variants and expands the phenotypic spectrum of PLK4-related primary microcephaly. In EUROPEAN JOURNAL OF HUMAN GENETICS (pp. 28-29). Milan, ITALY: LONDON: NATURE PUBLISHING GROUP.

MLA:

Boonsawat, Paranchai, et al. "Whole-exome sequencing identifies novel causative variants and expands the phenotypic spectrum of PLK4-related primary microcephaly." Proceedings of the 51st Conference of the European-Society-of-Human-Genetics (ESHG) in conjunction with the European Meeting on Psychosocial Aspects of Genetics (EMPAG), Milan, ITALY LONDON: NATURE PUBLISHING GROUP, 2019. 28-29.

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