Missense Med12 Variants In 22 Males With Intellectual Disability: From Non-Specific Symptoms To Complete Syndromes

AuthID
P-00Y-TH8
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
·
Hagen, JM
·
Tipo de Documento
Abstract
Year published
2023
Publicado
in MEDICINE, ISSN: 0025-7974
Volume: 102, Número: 13
Conference
26Th Annual Meeting of the Portuguese-Society-Of-Human-Genetics (Spgh), Date: NOV 17-19, 2022, Location: Coimbra, PORTUGAL
Indexing
Publication Identifiers
Wos: WOS:001005724900069
Source Identifiers
ISSN: 0025-7974
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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 Hagen, JM;
31 de Brouwer, APM;