Whole-exome sequencing identifies novel causative variants and expands the phenotypic spectrum of PLK4-related primary microcephaly - Boonsawat, Paranchai; Asadollahi, R.; Niedrist, D.; Joset, Pascal; Wisser, J.; Budka, H.; Bode, P. K.; Sticht, Heinrich; Steindl, K.; Rauch, Anita (EUROPEAN JOURNAL OF HUMAN GENETICS, 2019)
CRIS-Team WoS Importer:2021-10-18