Heterozygous Hmgb1 Loss-Of-Function Variants Are Associated with Developmental Delay and Microcephaly

AuthID
P-00V-3ZN
28
Author(s)
Krysiak, K
·
Audebert Bellanger, S
·
Redon, S
·
Benech, C
·
Viora Dupont, E
·
Mau Them, FT
·
Rondeau, S
·
[+1]·
[+3]·
[+4]·
Toutain, A
·
Bonneau, D
·
Gilbert Dussardier, B
·
Faivre, L
·
Rio, M
·
Le Marechal, C
·
Ferec, C
·
Repnikova, E
·
Cao, Y
Tipo de Documento
Article in Press
Year published
2021
Publicado
in CLINICAL GENETICS, ISSN: 0009-9163
Volume: 100, Número: 4, Páginas: 386-395 (10)
Indexing
Publication Identifiers
Pubmed: 34164801
SCOPUS: 2-s2.0-85114111824
Wos: WOS:000667160200001
Source Identifiers
ISSN: 0009-9163
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Name Order Nome   Name Order Nome   Name Order Nome
1 Uguen, K;   2 Krysiak, K;   3 Audebert Bellanger, S;
4 Redon, S;   5 Benech, C;   6 Viora Dupont, E;
7 Mau Them, FT;   8 Rondeau, S;   9 Elsharkawi, I;
10 Granadillo, JL;   11 Neidich, J;   12 Soares, CA;
13 Tkachenko, N;   14 Amudhavalli, SM;   15 Engleman, K;
16 Boland, A;   17 Deleuze, JF;   18 Bezieau, S;
19 Odent, S;   20 Toutain, A;   21 Bonneau, D;
22 Gilbert Dussardier, B;   23 Faivre, L;   24 Rio, M;
25 Le Marechal, C;   26 Ferec, C;   27 Repnikova, E;
28 Cao, Y;