Recommendations for whole genome sequencing in diagnostics for rare diseases

Summary

This is a publication. If there is no link to the publication on this page, you can try the pre-formated search via the search engines listed on this page.

Authors: Erika Souche Sergi Beltran, Erwin Brosens, John W Belmont, Magdalena Fossum, Olaf Riess, Christian Gilissen, Amin Ardeshirdavani, Gunnar Houge, Marielle van Gijn , Jill Clayton-Smith , Matthis Synofzik , Nicole de Leeuw, Zandra C Deans, Yasemin Dincer, Sebastian H Eck, Saskia van der Crabben, Meena Balasubramanian, Holm Graessner , Marc Sturm, Helen Firth, Alessandra Ferlini, Rima Nabbout, Elfrid

Journal title: Eur. J. Hum. Genet.

Journal number: Sep;30(9)

Journal publisher: European Journal of Human Genetics

Published year: 2022

Published pages: 1017-1021

DOI identifier: 10.1038/s41431-022-01113-x

ISSN: 1476-5438