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

AuthID
P-016-AY5
31
Author(s)
Ibarluzea, N
·
Misra‐Isrie, M
·
Koboldt, DC
·
Marques, I
·
Soares, G
·
Marcelis, CLM
·
Keski‐Filppula, R
·
Guitart, M
·
[+11]·
Abu‐Libde, B
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Kleefstra, T
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Elting, MW
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Császár, A
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Kárteszi, J
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Bessenyei, B
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van Bokhoven, H
·
Jorge, P
·
van Hagen, JM
·
de Brouwer, APM
Document Type
Article
Year published
2022
Published
in American Journal of Medical Genetics Part A, ISSN: 1552-4825
Volume: 191, Issue: 1, Pages: 135-143
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Source Identifiers
ISSN: 1552-4825
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Name Order Name   Name Order Name   Name Order Name
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 Gabau Vila, E;   12 Lehman, A;
13 Hickey, S;   14 Mori, M;   15 Terhal, P;
16 Valenzuela, I;   17 Lasa‐Aranzasti, A;   18 Cueto‐González, AM;
19 Chhouk, BH;   20 Yeh, RC;   21 Neil, JE;
22 Abu‐Libde, B;   23 Kleefstra, T;   24 Elting, MW;
25 Császár, A;   26 Kárteszi, J;   27 Bessenyei, B;
28 van Bokhoven, H;   29 Jorge, P;   30 van Hagen, JM;
31 de Brouwer, APM;