Crossmark

One test for all: whole exome sequencing significantly improves the diagnostic yield in growth retarded patients referred for molecular testing for Silver–Russell syndrome

Crossref DOI link: https://doi.org/10.1186/s13023-021-01683-x

Published Online: 2021-01-22

Published Print: 2021-12

Update policy: https://doi.org/10.1007/springer_crossmark_policy

Authors

Meyer, Robert

Begemann, Matthias

Hübner, Christian Thomas

Dey, Daniela

Kuechler, Alma

Elgizouli, Magdeldin

Schara, Ulrike

Ambrozaityte, Laima

Burnyte, Birute

Schröder, Carmen

Kenawy, Asmaa

Kroisel, Peter

Demuth, Stephanie

Fekete, Gyorgy

Opladen, Thomas

Elbracht, Miriam

Eggermann, Thomas https://orcid.org/0000-0002-8419-0264
Funding

Funding for this research was provided by:

Deutsche Forschungsgemeinschaft (EG110/15-1)

Projekt DEAL
License Information

Text and Data Mining valid from 2021-01-22

Version of Record valid from 2021-01-22
More Information

Article History

Received: 3 July 2020

Accepted: 6 January 2021

First Online: 22 January 2021

Ethics approval and consent to participate

: The study was approved by the ethical committee of the Medical Faculty of the RWTH Aachen (EK303-18).

: All participants gave their informed content for participation in this study.

: The authors declare that they have no competing interests.

Document is current

Any future updates will be listed below