Further Delineation of the Kbg Syndrome Caused by Ankrd11 Aberrations (Vol 23, Pg 1176, 2015)

AuthID
 P-00Y-DR5
24
Author(s)
Ockeloen, CW
·
Willemsen, MH
·
de Munnik, S
·
de Leeuw, N
·
Verrips, A
·
Kant, SG
·
Jones, EA
·
Brunner, HG
·
van Loon, RLE
·
[+4]·
Malmgren, H
·
Grigelioniene, G
·
Vermeer, S
·
Ramos, L
·
Maal, TJJ
·
van Heumen, CC
·
Yntema, HG
·
Carels, CEL
·
Kleefstra, T
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Document Type
Correction
Year published
2015
Published
in EUROPEAN JOURNAL OF HUMAN GENETICS, ISSN: 1018-4813
Volume: 23, Issue: 9, Pages: 1270-1270 (1)
Indexing
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Publication Identifiers
Pubmed: 26269249
Wos: WOS:000359448800029
Source Identifiers
ISSN: 1018-4813
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All authors
Name Order Name   Name Order Name   Name Order Name
1 Ockeloen, CW;   2 Willemsen, MH;   3 de Munnik, S;
4 van Bon, BWM;   5 de Leeuw, N;   6 Verrips, A;
7 Kant, SG;   8 Jones, EA;   9 Brunner, HG;
10 van Loon, RLE;   11 Smeets, EEJ;   12 van Haelst, MM;
13 van Haaften, G;   14 Nordgren, A;   15 Malmgren, H;
16 Grigelioniene, G;   17 Vermeer, S;   18 Louro, P ;
19 Ramos, L;   20 Maal, TJJ;   21 van Heumen, CC;
22 Yntema, HG;   23 Carels, CEL;   24 Kleefstra, T;

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