European recommendations for primary prevention of congenital anomalies: a joined effort of EUROCAT and EUROPLAN projects to facilitate inclusion of this topic in the National Rare Disease Plans

D Taruscio, L Arriola, F Baldi, I Barisic, E Bermejo-Sanchez, F Bianchi, E Calzolari, P Carbone, Rhonda M Curran, E Garne, M Gatt, A Latos-Bielenska, B Khoshnood, L Irgens, A Mantovani, ML Martinez-Frias, A Neville, A Rissmann, S Ruggeri, D Wellesley & 1 others Helen Dolk

    Research output: Contribution to journalArticle

    23 Citations (Scopus)
    LanguageEnglish
    Pages115-123
    JournalPublic Health Genomics
    Volume17
    Issue number2
    DOIs
    Publication statusPublished - Apr 2014

    Cite this

    Taruscio, D ; Arriola, L ; Baldi, F ; Barisic, I ; Bermejo-Sanchez, E ; Bianchi, F ; Calzolari, E ; Carbone, P ; Curran, Rhonda M ; Garne, E ; Gatt, M ; Latos-Bielenska, A ; Khoshnood, B ; Irgens, L ; Mantovani, A ; Martinez-Frias, ML ; Neville, A ; Rissmann, A ; Ruggeri, S ; Wellesley, D ; Dolk, Helen. / European recommendations for primary prevention of congenital anomalies: a joined effort of EUROCAT and EUROPLAN projects to facilitate inclusion of this topic in the National Rare Disease Plans. In: Public Health Genomics. 2014 ; Vol. 17, No. 2. pp. 115-123.
    @article{32f3e2e016db4b99a0ace21caadf0e7c,
    title = "European recommendations for primary prevention of congenital anomalies: a joined effort of EUROCAT and EUROPLAN projects to facilitate inclusion of this topic in the National Rare Disease Plans",
    author = "D Taruscio and L Arriola and F Baldi and I Barisic and E Bermejo-Sanchez and F Bianchi and E Calzolari and P Carbone and Curran, {Rhonda M} and E Garne and M Gatt and A Latos-Bielenska and B Khoshnood and L Irgens and A Mantovani and ML Martinez-Frias and A Neville and A Rissmann and S Ruggeri and D Wellesley and Helen Dolk",
    year = "2014",
    month = "4",
    doi = "10.1159/000360602",
    language = "English",
    volume = "17",
    pages = "115--123",
    journal = "Public Health Genomics",
    issn = "1662-4246",
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    Taruscio, D, Arriola, L, Baldi, F, Barisic, I, Bermejo-Sanchez, E, Bianchi, F, Calzolari, E, Carbone, P, Curran, RM, Garne, E, Gatt, M, Latos-Bielenska, A, Khoshnood, B, Irgens, L, Mantovani, A, Martinez-Frias, ML, Neville, A, Rissmann, A, Ruggeri, S, Wellesley, D & Dolk, H 2014, 'European recommendations for primary prevention of congenital anomalies: a joined effort of EUROCAT and EUROPLAN projects to facilitate inclusion of this topic in the National Rare Disease Plans', Public Health Genomics, vol. 17, no. 2, pp. 115-123. https://doi.org/10.1159/000360602

    European recommendations for primary prevention of congenital anomalies: a joined effort of EUROCAT and EUROPLAN projects to facilitate inclusion of this topic in the National Rare Disease Plans. / Taruscio, D; Arriola, L; Baldi, F; Barisic, I; Bermejo-Sanchez, E; Bianchi, F; Calzolari, E; Carbone, P; Curran, Rhonda M; Garne, E; Gatt, M; Latos-Bielenska, A; Khoshnood, B; Irgens, L; Mantovani, A; Martinez-Frias, ML; Neville, A; Rissmann, A; Ruggeri, S; Wellesley, D; Dolk, Helen.

    In: Public Health Genomics, Vol. 17, No. 2, 04.2014, p. 115-123.

    Research output: Contribution to journalArticle

    TY - JOUR

    T1 - European recommendations for primary prevention of congenital anomalies: a joined effort of EUROCAT and EUROPLAN projects to facilitate inclusion of this topic in the National Rare Disease Plans

    AU - Taruscio, D

    AU - Arriola, L

    AU - Baldi, F

    AU - Barisic, I

    AU - Bermejo-Sanchez, E

    AU - Bianchi, F

    AU - Calzolari, E

    AU - Carbone, P

    AU - Curran, Rhonda M

    AU - Garne, E

    AU - Gatt, M

    AU - Latos-Bielenska, A

    AU - Khoshnood, B

    AU - Irgens, L

    AU - Mantovani, A

    AU - Martinez-Frias, ML

    AU - Neville, A

    AU - Rissmann, A

    AU - Ruggeri, S

    AU - Wellesley, D

    AU - Dolk, Helen

    PY - 2014/4

    Y1 - 2014/4

    U2 - 10.1159/000360602

    DO - 10.1159/000360602

    M3 - Article

    VL - 17

    SP - 115

    EP - 123

    JO - Public Health Genomics

    T2 - Public Health Genomics

    JF - Public Health Genomics

    SN - 1662-4246

    IS - 2

    ER -