The Koolen-De Vries Syndrome: a Phenotypic Comparison of Patients with a 17Q21.31 Microdeletion Versus a Kansl1 Sequence Variant

AuthID
P-00K-HR0
49
Author(s)
Pfundt, R
·
Linda, K
·
Beunders, G
·
Veenstra Knol, HE
·
Conta, JH
·
[+1]·
[+17]·
[+2]·
[+3]·
[+2]·
[+4]·
Thompson, EM
·
Romano, C
·
Eichler, EE
·
de Vries, BBA
1
Group Author(s)
DDD Study
Tipo de Documento
Article
Year published
2016
Publicado
in EUROPEAN JOURNAL OF HUMAN GENETICS, ISSN: 1018-4813
Volume: 24, Número: 5, Páginas: 652-659 (8)
Indexing
Publication Identifiers
SCOPUS: 2-s2.0-84963955091
Wos: WOS:000374125200008
Source Identifiers
ISSN: 1018-4813
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Name Order Nome   Name Order Nome   Name Order Nome
1 Koolen, DA;   2 Pfundt, R;   3 Linda, K;
4 Beunders, G;   5 Veenstra Knol, HE;   6 Conta, JH;
7 Fortuna, AM;   8 Gillessen Kaesbach, G;   9 Dugan, S;
10 Halbach, S;   11 Abdul Rahman, OA;   12 Winesett, HM;
13 Chung, WK;   14 Dalton, M;   15 Dimova, PS;
16 Mattina, T;   17 Prescott, K;   18 Zhang, HZ;
19 Saal, HM;   20 Hehir Kwa, JY;   21 Willemsen, MH;
22 Ockeloen, CW;   23 Jongmans, MC;   24 Van der Aa, N;
25 Failla, P;   26 Barone, C;   27 Avola, E;
28 Brooks, AS;   29 Kant, SG;   30 Gerkes, EH;
31 Firth, HV;   32 Ounap, K;   33 Bird, LM;
34 Masser Frye, D;   35 Friedman, JR;   36 Sokunbi, MA;
37 Dixit, A;   38 Splitt, M;   39 Kukolich, MK;
40 McGaughran, J;   41 Coe, BP;   42 Florez, J;
43 Kasri, NN;   44 Brunner, HG;   45 Thompson, EM;
46 Gecz, J;   47 Romano, C;   48 Eichler, EE;
49 de Vries, BBA;