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The Koolen-De Vries Syndrome: a Phenotypic Comparison of Patients with a 17Q21.31 Microdeletion Versus a Kansl1 Sequence Variant
AuthID
P-00K-HR0
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
Document Type
Article
Year published
2016
Published
in EUROPEAN JOURNAL OF HUMAN GENETICS, ISSN: 1018-4813
Volume: 24, Issue: 5, Pages: 652-659 (8)
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ISSN: 1018-4813
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| Name Order | Name | Name Order | Name | Name Order | Name | ||
|---|---|---|---|---|---|---|---|
| 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; |
