Missing/wrong data?
Log in to edit
Whole-exome analysis of foetal autopsy tissue reveals a frameshift mutation in OBSL1, consistent with a diagnosis of 3-M Syndrome
scientific article
Author/s
author: Stephen W. Scherer, Richard F Wintle, Sergio L Pereira, Muhammad Abu-Elmagd, Tracy Stockley
Work details
Publication date
January 15, 2015
-
-
Language
English
Copyright status
Copyright status information is not available for this work. The copyright status depends on the jurisdiction, the author's date of death and the date the work was created or published.
To learn more about copyright terms in different countries, visit the countries and terms page.