1. The first familial case of inherited 2q37.3 interstitial deletion with isolated skeletal abnormalities including brachydactyly type E and short stature. (17th November 2014) Authors: Jean‐Marçais, Nolwenn; Decamp, Matthieu; Gérard, Marion; Ribault, Virginie; Andrieux, Joris; Kottler, Marie‐Laure; Plessis, Ghislaine Journal: American journal of medical genetics Issue: Volume 167:Number 1(2015:Jan.) Page Start: 185 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗