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Willmott, Lindy, White, Ben, Feeney, Rachel, Chambaere, Kenneth, Yates, Patsy, Mitchell, Geoffrey
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Chambaere, Kenneth, Rietjens, Judith AC, Cohen, Joachim, Pardon, Koen, Deschepper, Reginald, Pasman, H Roeline W, Deliens, Luc
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Dommering, Charlotte J., Henneman, Lidewij, van der Hout, Annemarie H., Jonker, Marianne A., Tops, Carli M. J., van den Ouweland, Ans M. W., van der Luijt, Rob B., Mensenkamp, Arjen R., Hogervorst, Frans B. L., Redeker, Egbert J. W., de Die-Smulders, Christine E. M., Moll, Annette C., Meijers-Heijboer, Hanne
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Veröffentlicht in: Dommering , C J , Henneman , L , van der Hout , A H , Jonker , M A , Tops , C M J , van den Ouweland , A M W , van der Luijt , R B , Mensenkamp , A R , Hogervorst , F B L , Redeker , E J W , de Die-Smulders , C E M , Moll , A C & Meijers-Heijboer , H 2017 , ' Uptake of prenatal diagnostic testing for retinoblastoma compared to other hereditary cancer syndromes in the Netherlands ' , Familial Cancer , vol. 16 , no. 2 , pp. 271-277 . https://doi.org/10.1007/s10689-016-9943-z;
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