Primrose syndrome: a phenotypic comparison of patients with a ZBTB20 single-nucleotide variant versus a 3q13.31 microdeletion including ZBTB20

Juven, A; Nambot, S; Piton, A; Callier, P; Philippe, C; Jean-Marcais, N; Munnich, A; Rio, M; Colleaux, L; Rondeau, S; Steffann, J; Attie-Bitach, T; Thomas, S; El Chehadeh, S; Delorme, CV; Bouquillon, S; Francannet, C; Laffargue, F; Gouas, L; Blesson,

EUROPEAN JOURNAL OF HUMAN GENETICS, 2019; 27 (): 377

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