Missense Med12 Variants in 22 Males with Intellectual Disability: From Nonspecific Symptoms to Complete Syndromes

AuthID
P-00X-E0E
31
Author(s)
Maia, N
·
Ibarluzea, N
·
Misra-Isrie, M
·
Koboldt, DC
·
Marques, I
·
Soares, G
·
Santos, R
·
[+3]·
[+2]·
[+2]·
[+4]·
Csaszar, A
·
van Bokhoven, H
·
Jorge, P
·
van Hagen, JM
·
de Brouwer, APM
Tipo de Documento
Article in Press
Year published
2022
Publicado
in AMERICAN JOURNAL OF MEDICAL GENETICS PART A, ISSN: 1552-4825
Indexing
Publication Identifiers
Pubmed: 36271811
SCOPUS: 2-s2.0-85140230561
Wos: WOS:000871026600001
Source Identifiers
ISSN: 1552-4825
Export Publication Metadata
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Name Order Nome   Name Order Nome   Name Order Nome
1 Maia, N;   2 Ibarluzea, N;   3 Misra-Isrie, M;
4 Koboldt, DC;   5 Marques, I;   6 Soares, G;
7 Santos, R;   8 Marcelis, CLM;   9 Keski-Filppula, R;
10 Guitart, M;   11 Vila, EG;   12 Lehman, A;
13 Hickey, S;   14 Mori, M;   15 Terhal, P;
16 Valenzuela, I;   17 Lasa-Aranzasti, A;   18 Cueto-Gonzalez, AM;
19 Chhouk, BH;   20 Yeh, RC;   21 Neil, JE;
22 Abu-Libde, B;   23 Kleefstra, T;   24 Elting, MW;
25 Csaszar, A;   26 Karteszi, J;   27 Bessenyei, B;
28 van Bokhoven, H;   29 Jorge, P;   30 van Hagen, JM;
31 de Brouwer, APM;