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Surveillance of Multiple Congenital Anomalies; Searching for New Associations
AuthID
P-00Z-FW3
P-00Z-FW3
28
Author(s)
Morris, JK
·Bergman, JEH
·Barisic, I
·Limb, E
·[+2]·
[+1]·
[+1]·
[+1]·
[+2]·
[+1]·
Sayers, G
·Kinsner Ovaskainen, A
·Tipo de Documento
Article in Press
Year published
2023
Publicado
in EUROPEAN JOURNAL OF HUMAN GENETICS, ISSN: 1018-4813
Indexing
Publication Identifiers
Pubmed: 38052905
SCOPUS: 2-s2.0-85178447193
Wos: WOS:001114313300003
Source Identifiers
ISSN: 1018-4813
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| Name Order | Nome | Name Order | Nome | Name Order | Nome | ||
|---|---|---|---|---|---|---|---|
| 1 | Morris, JK; | 2 | Bergman, JEH; | 3 | Barisic, I; | ||
| 4 | Wellesley, D; | 5 | Tucker, D; | 6 | Limb, E; | ||
| 7 | Addor, MC; | 8 | Cavero Carbonell, C; | 9 | Dias, CM; | ||
| 10 | Draper, ES; | 11 | Echevarría González de Garibay, LJ; | 12 | Gatt, M; | ||
| 13 | Klungsoyr, K; | 14 | Lelong, N; | 15 | Luyt, K; | ||
| 16 | Materna Kiryluk, A; | 17 | Nelen, V; | 18 | Neville, A; | ||
| 19 | Perthus, I; | 20 | Pierini, A; | 21 | Randrianaivo Ranjatoelina, H; | ||
| 22 | Rankin, J; | 23 | Rissmann, A; | 24 | Rouget, F; | ||
| 25 | Sayers, G; | 26 | Wertelecki, W; | 27 | Kinsner Ovaskainen, A; | ||
| 28 | Garne, E; |
