Redefining the Med13L Syndrome

AuthID
 P-00G-QJT
32
Author(s)
Adegbola, A
·
Hu, H
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[+2]·
[+1]·
[+1]·
[+3]·
[+2]·
[+1]·
[+2]·
Ropers, HH
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Hubner, C
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Kaindl, AM
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Document Type
Article
Year published
2015
Published
in EUROPEAN JOURNAL OF HUMAN GENETICS, ISSN: 1018-4813
Volume: 23, Issue: 10, Pages: 1308-1317 (10)
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Publication Identifiers
Scopus: 2-s2.0-84944171575
Wos: WOS:000361747700008
Source Identifiers
ISSN: 1018-4813
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All authors
Name Order Name   Name Order Name   Name Order Name
1 Adegbola, A;   2 Musante, L;   3 Callewaert, B;
4 Maciel, P;   5 Hu, H;   6 Isidor, B;
7 Picker Minh, S;   8 Le Caignec, C;   9 Delle Chiaie, B;
10 Vanakker, O;   11 Menten, B;   12 Dheedene, A;
13 Bockaert, N;   14 Roelens, F;   15 Decaestecker, K;
16 Silva, J;   17 Soares, G;   18 Lopes, F;
19 Najmabadi, H;   20 Kahrizi, K;   21 Cox, GF;
22 Angus, SP;   23 Staropoli, JF;   24 Fischer, U;
25 Suckow, V;   26 Bartsch, O;   27 Chess, A;
28 Ropers, HH;   29 Wienker, TF;   30 Hubner, C;
31 Kaindl, AM;   32 Kalscheuer, VM;  

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