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Nedeljkovic, Ivana, Terzikhan, Natalie, Vonk, Judith M., van der Plaat, Diana A., Lahousse, Lies, van Diemen, Cleo C., Hobbs, Brian D., Qiao, Dandi, Cho, Michael H., Brusselle, Guy G., Postma, Dirkje S., Boezen, H. M., van Duijn, Cornelia M., Amin, Najaf
Veröffentlicht in: Nedeljkovic , I , Terzikhan , N , Vonk , J M , van der Plaat , D A , Lahousse , L , van Diemen , C C , Hobbs , B D , Qiao , D , Cho , M H , Brusselle , G G , Postma , D S , Boezen , H M , van Duijn , C M & Amin , N 2018 , ' A Genome-Wide Linkage Study for Chronic Obstructive Pulmonary Disease in a Dutch Genetic Isolate Identifies Novel Rare Candidate Variants ' , Frontiers in Genetics , vol. 9 , 133 . https://doi.org/10.3389/fgene.2018.00133;
2018
Veröffentlicht in: Nedeljkovic , I , Terzikhan , N , Vonk , J M , van der Plaat , D A , Lahousse , L , van Diemen , C C , Hobbs , B D , Qiao , D , Cho , M H , Brusselle , G G , Postma , D S , Boezen , H M , van Duijn , C M & Amin , N 2018 , ' A Genome-Wide Linkage Study for Chronic Obstructive Pulmonary Disease in a Dutch Genetic Isolate Identifies Novel Rare Candidate Variants ' , Frontiers in Genetics , vol. 9 , 133 . https://doi.org/10.3389/fgene.2018.00133;
2018
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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
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