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Redefining the Med13L Syndrome
AuthID
P-00G-QJT
P-00G-QJT
32
Author(s)
Adegbola, A
·Hu, H
·[+2]·
[+1]·
[+1]·
[+3]·
[+2]·
[+1]·
[+2]·
Ropers, HH
·Hubner, C
·Kaindl, AM
·Document Type
Article
Year published
2015
Published
in EUROPEAN JOURNAL OF HUMAN GENETICS, ISSN: 1018-4813
Volume: 23, Issue: 10, Pages: 1308-1317 (10)
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ISSN: 1018-4813
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| Name Order | Name | Name Order | Name | Name Order | Name | ||
|---|---|---|---|---|---|---|---|
| 1 | Adegbola, A; | 2 | Musante, L; | 3 | Callewaert, B; | ||
| 4 | Maciel, P; | 5 | Hu, H; | 6 | Isidor, B; | ||
| 7 | Picker Minh, S; | 8 | Le Caignec, C; | 9 | Delle Chiaie, B; | ||
| 10 | Vanakker, O; | 11 | Menten, B; | 12 | Dheedene, A; | ||
| 13 | Bockaert, N; | 14 | Roelens, F; | 15 | Decaestecker, K; | ||
| 16 | Silva, J; | 17 | Soares, G; | 18 | Lopes, F; | ||
| 19 | Najmabadi, H; | 20 | Kahrizi, K; | 21 | Cox, GF; | ||
| 22 | Angus, SP; | 23 | Staropoli, JF; | 24 | Fischer, U; | ||
| 25 | Suckow, V; | 26 | Bartsch, O; | 27 | Chess, A; | ||
| 28 | Ropers, HH; | 29 | Wienker, TF; | 30 | Hubner, C; | ||
| 31 | Kaindl, AM; | 32 | Kalscheuer, VM; |
