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van Leersum, Frank S., Nagtzaam, Ivo F., van Oosterhoud, Carolien N., Ghesquiere, Stijn A. I., Brandts, Roel R. H. F. J., Gostynski, Antoni, Steijlen, Peter M., van Geel, Michel
Veröffentlicht in: van Leersum , F S , Nagtzaam , I F , van Oosterhoud , C N , Ghesquiere , S A I , Brandts , R R H F J , Gostynski , A , Steijlen , P M & van Geel , M 2020 , ' Improving the diagnostic yield for filaggrin : Concealed mutations in the Dutch population ' , Journal of Allergy and Clinical Immunology , vol. 145 , no. 6 , pp. 1704 . https://doi.org/10.1016/j.jaci.2020.01.033;
2020
Veröffentlicht in: van Leersum , F S , Nagtzaam , I F , van Oosterhoud , C N , Ghesquiere , S A I , Brandts , R R H F J , Gostynski , A , Steijlen , P M & van Geel , M 2020 , ' Improving the diagnostic yield for filaggrin : Concealed mutations in the Dutch population ' , Journal of Allergy and Clinical Immunology , vol. 145 , no. 6 , pp. 1704 . https://doi.org/10.1016/j.jaci.2020.01.033;
2020
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Van Opstal, Diane, van Maarle, Merel C., Lichtenbelt, Klaske, Weiss, Marjan M., Schuring-Blom, Heleen, Bhola, Shama L., Hoffer, Mariette J. V., Huijsdens-van Amsterdam, Karin, Macville, Merryn V., Kooper, Angelique J. A., Faas, Brigitte H. W., Govaerts, Lutgarde, Tan-Sindhunata, Gita M., den Hollander, Nicolette, Feenstra, Ilse, Galjaard, Robert-Jan H., Oepkes, Dick, Ghesquiere, Stijn, Brouwer, Rutger W. W., Beulen, Lean, Bollen, Sander, Elferink, Martin G., Straver, Roy, Henneman, Lidewij, Page-Christiaens, Godelieve C., Sistermans, Erik A.
Veröffentlicht in: Van Opstal , D , van Maarle , M C , Lichtenbelt , K , Weiss , M M , Schuring-Blom , H , Bhola , S L , Hoffer , M J V , Huijsdens-van Amsterdam , K , Macville , M V , Kooper , A J A , Faas , B H W , Govaerts , L , Tan-Sindhunata , G M , den Hollander , N , Feenstra , I , Galjaard , R-J H , Oepkes , D , Ghesquiere , S , Brouwer , R W W , Beulen , L , Bollen , S , Elferink , M G , Straver , R , Henneman , L , Page-Christiaens , G C , Sistermans , E A & Dutch NIPT Consortium 2018 , ' Origin and clinical relevance of chromosomal aberrations other than the common trisomies detected by genome-wide NIPS: results of the TRIDENT study ' , Genetics in Medicine , vol. 20 , no. 5 , pp. 480-485 . https://doi.org/10.1038/gim.2017.132;
2018
Veröffentlicht in: Van Opstal , D , van Maarle , M C , Lichtenbelt , K , Weiss , M M , Schuring-Blom , H , Bhola , S L , Hoffer , M J V , Huijsdens-van Amsterdam , K , Macville , M V , Kooper , A J A , Faas , B H W , Govaerts , L , Tan-Sindhunata , G M , den Hollander , N , Feenstra , I , Galjaard , R-J H , Oepkes , D , Ghesquiere , S , Brouwer , R W W , Beulen , L , Bollen , S , Elferink , M G , Straver , R , Henneman , L , Page-Christiaens , G C , Sistermans , E A & Dutch NIPT Consortium 2018 , ' Origin and clinical relevance of chromosomal aberrations other than the common trisomies detected by genome-wide NIPS: results of the TRIDENT study ' , Genetics in Medicine , vol. 20 , no. 5 , pp. 480-485 . https://doi.org/10.1038/gim.2017.132;
2018