Expanding the mutation and clinical spectrum of Roberts syndrome

In conclusion, we report a novel ESCO2 mutation and expand the clinical spectrum of Roberts syndrome. This article is protected by copyright. All rights reserved.

Source: Congenital Anomalies - December 29, 2015 Category: Genetics & Stem Cells Authors: Hanan H. Afifi, Ghada M.H. Abdel‐Salam, Maha M. Eid, Angie M.S. Tosson, Wafaa Gh. Shousha, Amira A. Abdel Azeem, Mona K. Farag, Mennat I. Mehrez, Khaled R. Gaber Tags: Original Article Source Type: research