AXIN1 bi-allelic variants disrupting the C-terminal DIX domain cause craniometadiaphyseal osteosclerosis with hip dysplasia - Terhal, Paulien; Venhuizen, Anton J.; Lessel, Davor; Tan, Wen-Hann; Alswaid, Abdulrahman; Grün, Regina; Alzaidan, Hamad I.; von Kroge, Simon; Ragab, Nada; Hempel, Maja; Kubisch, Christian; Novais, Eduardo; et al. (The American journal of human genetics, 2023)
Online verfügbar: 14. August 2023, Artikelversion: 7. September 2023