1. Myeloid malignancies with translocation t(4;12)(q11‐13;p13): molecular landscape, clonal hierarchy and clinical outcomes. Issue 20 (7th September 2021) Authors: Parinet, Vincent; Chapiro, Elise; Bidet, Audrey; Gaillard, Baptiste; Maarek, Odile; Simon, Laurence; Lefebvre, Christine; Defasque, Sabine; Mozziconacci, Marie‐Joelle; Quinquenel, Anne; Decamp, Matthieu; Lifermann, François; Ali‐Ammar, Nadia; Maillon, Agathe; Baron, Marine; Martin, Mélanie; Strus... Journal: Journal of cellular and molecular medicine Issue: Volume 25:Issue 20(2021) Page Start: 9557 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. 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) ↗