J. Neidich
AuthID: R-00K-00R
1
TITLE: Heterozygous HMGB1 loss-of-function variants are associated with developmental delay and microcephaly Full Text
AUTHORS: Uguen, K; Krysiak, K; Audebert Bellanger, S; Redon, S; Benech, C; Viora Dupont, E; Mau Them, FT; Rondeau, S; Elsharkawi, I; Granadillo, JL; Neidich, J; Soares, CA; Tkachenko, N; Amudhavalli, SM; Engleman, K; Boland, A; Deleuze, JF; Bezieau, S; Odent, S; Toutain, A; ...More
PUBLISHED: 2021, SOURCE: CLINICAL GENETICS, VOLUME: 100, ISSUE: 4
AUTHORS: Uguen, K; Krysiak, K; Audebert Bellanger, S; Redon, S; Benech, C; Viora Dupont, E; Mau Them, FT; Rondeau, S; Elsharkawi, I; Granadillo, JL; Neidich, J; Soares, CA; Tkachenko, N; Amudhavalli, SM; Engleman, K; Boland, A; Deleuze, JF; Bezieau, S; Odent, S; Toutain, A; ...More
PUBLISHED: 2021, SOURCE: CLINICAL GENETICS, VOLUME: 100, ISSUE: 4
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