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De Novo Cltc Variants Are Associated with a Variable Phenotype from Mild to Severe Intellectual Disability, Microcephaly, Hypoplasia of the Corpus Callosum, and Epilepsy
AuthID
P-015-D99
P-015-D99
30
Author(s)
Venselaar, H
·Wiel, L
·Trimouille, A
·Lasseaux, E
·Naudion, S
·Lacombe, D
·Piton, A
·Vincent-Delorme, C
·Zweier, C
·[+10]·
Bijlsma, EK
·Barakat, TS
·van Dooren, MF
·van Slegtenhorst, M
·Pfundt, R
·Gilissen, C
·Willemsen, MA
·de Vries, BB
·de Brouwer, AP
·Koolen, DA
Tipo de Documento
Article
Year published
2020
Publicado
in Genetics in Medicine, ISSN: 1098-3600
Volume: 22, Número: 4, Páginas: 797-802
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ISSN: 1098-3600
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| Name Order | Nome | Name Order | Nome | Name Order | Nome | ||
|---|---|---|---|---|---|---|---|
| 1 | Nabais Sá, MJ; | 2 | Venselaar, H; | 3 | Wiel, L; | ||
| 4 | Trimouille, A; | 5 | Lasseaux, E; | 6 | Naudion, S; | ||
| 7 | Lacombe, D; | 8 | Piton, A; | 9 | Vincent-Delorme, C; | ||
| 10 | Zweier, C; | 11 | Reis, A; | 12 | Trollmann, R; | ||
| 13 | Ruiz, A; | 14 | Gabau, E; | 15 | Vetro, A; | ||
| 16 | Guerrini, R; | 17 | Bakhtiari, S; | 18 | Kruer, MC; | ||
| 19 | Amor, DJ; | 20 | Cooper, MS; | 21 | Bijlsma, EK; | ||
| 22 | Barakat, TS; | 23 | van Dooren, MF; | 24 | van Slegtenhorst, M; | ||
| 25 | Pfundt, R; | 26 | Gilissen, C; | 27 | Willemsen, MA; | ||
| 28 | de Vries, BB; | 29 | de Brouwer, AP; | 30 | Koolen, DA; |
