Missense Variants in Taf1 and Developmental Phenotypes: Challenges of Determining Pathogenicity

AuthID
P-00R-DQE
56
Author(s)
Cheng, HY
·
Capponi, S
·
Wakeling, E
·
Marchi, E
·
Li, Q
·
Zhao, MG
·
Weng, CH
·
Stefan, PG
·
Ahlfors, H
·
Kleyner, R
·
[+21]·
[+15]·
Ades, LC
·
Sandaradura, SA
·
Lupski, JR
·
Roscioli, T
·
Agrawal, PB
·
Kline, AD
·
Wang, K
·
Timmers, HTM
·
Lyon, GJ
1
Group Author(s)
Deciphering Dev Disorders Study
Document Type
Article
Year published
2020
Published
in HUMAN MUTATION, ISSN: 1059-7794
Volume: 41, Issue: 2, Pages: 449-464 (16)
Indexing
Publication Identifiers
SCOPUS: 2-s2.0-85075484672
Wos: WOS:000498296700001
Source Identifiers
ISSN: 1059-7794
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Name Order Name   Name Order Name   Name Order Name
1 Cheng, HY;   2 Capponi, S;   3 Wakeling, E;
4 Marchi, E;   5 Li, Q;   6 Zhao, MG;
7 Weng, CH;   8 Stefan, PG;   9 Ahlfors, H;
10 Kleyner, R;   11 Rope, A;   12 Lumaka, A;
13 Lukusa, P;   14 Devriendt, K;   15 Vermeesch, J;
16 Posey, JE;   17 Palmer, EE;   18 Murray, L;
19 Leon, E;   20 Diaz, J;   21 Worgan, L;
22 Mallawaarachchi, A;   23 Vogt, J;   24 de Munnik, SA;
25 Dreyer, L;   26 Baynam, G;   27 Ewans, L;
28 Stark, Z;   29 Lunke, S;   30 Goncalves, AR;
31 Soares, G;   32 Oliveira, J;   33 Fassi, E;
34 Willing, M;   35 Waugh, JL;   36 Faivre, L;
37 Riviere, JB;   38 Moutton, S;   39 Mohammed, S;
40 Payne, K;   41 Walsh, L;   42 Begtrup, A;
43 Sacoto, MJG;   44 Douglas, G;   45 Alexander, N;
46 Buckley, MF;   47 Mark, PR;   48 Ades, LC;
49 Sandaradura, SA;   50 Lupski, JR;   51 Roscioli, T;
52 Agrawal, PB;   53 Kline, AD;   54 Wang, K;
55 Timmers, HTM;   56 Lyon, GJ;