Shovlin, C. L ;
Buscarini, E ;
Sabbà, C...
Shovlin , C L , Buscarini , E , Sabbà , C , Mager , H J , Kjeldsen , A D , Pagella , F , Sure , U , Ugolini , S , Torring , P M , Suppressa , P , Rennie , C , Post , M C , Patel , M C , Nielsen , T H , Manfredi , G , Lenato , G M , Lefroy , D , Kariholu , U , Jones , B , Fialla , A D , Eker , O F , Dupuis , O , Droege , F , Coote , N , Boccardi , E , Alsafi , A , Alicante , S & Dupuis-Girod , S 2022 , ' The European Rare Disease Network for HHT Frameworks for management of hereditary haemorrhagic telangiectasia in general and speciality care ' , European Journal of Medical Genetics , vol. 65 , no. 1 , 104370 . https://doi.org/10.1016/j.ejmg.2021.104370.
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2022