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Further Delineation of the Kbg Syndrome Phenotype Caused by Ankrd11 Aberrations
AuthID
P-00G-FYB
P-00G-FYB
24
Author(s)
Ockeloen, CW
·Willemsen, MH
·de Munnik, S
·de Leeuw, N
·Jones, EA
·van Loon, RLE
·[+1]·
[+3]·
·
van Heumen, CC
·Yntema, HG
·Carels, CEL
·Kleefstra, T
Tipo de Documento
Article
Year published
2015
Publicado
in EUROPEAN JOURNAL OF HUMAN GENETICS, ISSN: 1018-4813
Volume: 23, Número: 9, Páginas: 1176-1185 (10)
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ISSN: 1018-4813
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| Name Order | Nome | Name Order | Nome | Name Order | Nome | ||
|---|---|---|---|---|---|---|---|
| 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; |
