Primrose syndrome: a phenotypic comparison of patients with a ZBTB20 missense variant versus a 3q13.31 microdeletion including ZBTB20. - Juven A; Nambot S; Piton A; Jean-Marçais N; Masurel A; Callier P; Marle N; Mosca-Boidron AL; Kuentz P; Philippe C; Chevarin M; Duffourd Y; et al. (European journal of human genetics : EJHG, 2020)