De novo mutations in FBRSL1 cause a novel recognizable malformation and intellectual disability syndrome
- Resource Type
- Journal
- Authors
- Ufartes, Roser; Berger, Hanna; Till, Katharina; Salinas, Gabriela; Sturm, Marc; Altmueller, Janine; Nuernberg, Peter; Thiele, Holger; Funke, Rudolf; Apeshiotis, Neophytos; Langen, Hendrik; Wollnik, Bernd; Borchers, Annette; Pauli, Silke
- Source
- HUMAN GENETICS; MAY 18 2020, 17p.
- Subject
- Language
- English
- ISSN
- 14321203