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pro vyhledávání: '"Ghesquiere, S."'
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Autor:
Opstal, D. van, Maarle, M.C. van, 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., Hollander, N. den, 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
Publikováno v:
Genetics in Medicine, 20, 480-485
Genetics in Medicine
Genetics in Medicine, 20(5), 480-485. Nature Publishing Group
Genetics in medicine, 20(5), 480-485. Lippincott Williams and Wilkins
Genetics in Medicine, 20(5), 480-485. Lippincott Williams and Wilkins
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 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, https://doi.org/10.1038/gim.2017.132
Genetics in Medicine, 20, 5, pp. 480-485
Genetics in Medicine, 20(5), 480-485
Genetics in Medicine, 20(5), 480-485. Lippincott Williams & Wilkins
Genetics in Medicine
Genetics in Medicine, 20(5), 480-485. Nature Publishing Group
Genetics in medicine, 20(5), 480-485. Lippincott Williams and Wilkins
Genetics in Medicine, 20(5), 480-485. Lippincott Williams and Wilkins
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 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, https://doi.org/10.1038/gim.2017.132
Genetics in Medicine, 20, 5, pp. 480-485
Genetics in Medicine, 20(5), 480-485
Genetics in Medicine, 20(5), 480-485. Lippincott Williams & Wilkins
PurposeNoninvasive prenatal screening (NIPS) using cell-free DNA in maternal blood is highly sensitive for detecting fetal trisomies 21, 18, and 13. Using a genome-wide approach, other chromosome anomalies can also be detected. We report on the origi
Autor:
Li, Jing-Wen1 (AUTHOR), Qian, Yan-Jie1 (AUTHOR), Mao, Shao-Jia1 (AUTHOR), Chao, Yun-Qi1 (AUTHOR), Qin, Yi-Fang1 (AUTHOR), Hu, Chen-Xi1 (AUTHOR), Li, Zheng-Lan1,2 (AUTHOR), Zou, Chao-Chun1 (AUTHOR) zcc14@zju.edu.cn
Publikováno v:
Molecular Cytogenetics (17558166). 7/29/2024, Vol. 17 Issue 1, p1-6. 6p.
Autor:
Chen, Shuai1 (AUTHOR), Lu, Zhi2,3 (AUTHOR), Zhao, Yudong4 (AUTHOR), Xia, Lu1 (AUTHOR), Liu, Chun1 (AUTHOR), Zuo, Siqing2,3 (AUTHOR), Jin, Manchang3,5 (AUTHOR), Jia, Haoyu1 (AUTHOR), Li, Shanshan1 (AUTHOR), Zhang, Shuo1 (AUTHOR), Yang, Bo1 (AUTHOR), Wang, Zhijing1 (AUTHOR), Li, Jing1 (AUTHOR) li.jing@tongji.edu.cn, Wang, Fei6 (AUTHOR) wangf323@mail.sysu.edu.cn, Yang, Changqing1 (AUTHOR) cqyang@tongji.edu.cn
Publikováno v:
Advanced Science. Apr2024, Vol. 11 Issue 16, p1-20. 20p.
Autor:
Van Opstal D; Department of Clinical Genetics, Erasmus Medical Center, Rotterdam, The Netherlands., van Maarle MC; Department of Clinical Genetics, Academic Medical Center, Amsterdam, Amsterdam, The Netherlands., Lichtenbelt K; Department of Genetics, University Medical Center Utrecht, Utrecht, The Netherlands., Weiss MM; Department of Clinical Genetics, VU University Medical Center, Amsterdam, The Netherlands., Schuring-Blom H; Department of Genetics, University Medical Center Utrecht, Utrecht, The Netherlands., Bhola SL; Department of Clinical Genetics, VU University Medical Center, Amsterdam, The Netherlands., Hoffer MJV; Department of Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands., Huijsdens-van Amsterdam K; Department of Clinical Genetics, Academic Medical Center, Amsterdam, Amsterdam, The Netherlands., Macville MV; Department of Clinical Genetics, Maastricht UMC+, Maastricht, The Netherlands., Kooper AJA; Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands., Faas BHW; Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands., Govaerts L; Department of Clinical Genetics, Erasmus Medical Center, Rotterdam, The Netherlands., Tan-Sindhunata GM; Department of Clinical Genetics, VU University Medical Center, Amsterdam, The Netherlands., den Hollander N; Department of Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands., Feenstra I; Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands., Galjaard RH; Department of Clinical Genetics, Erasmus Medical Center, Rotterdam, The Netherlands., Oepkes D; Department of Obstetrics, Leiden University Medical Center, Leiden, The Netherlands., Ghesquiere S; Department of Clinical Genetics, Maastricht UMC+, Maastricht, The Netherlands., Brouwer RWW; Erasmus Center for Biomics, Erasmus Medical Center, Rotterdam, The Netherlands., Beulen L; Department of Obstetrics and Gynaecology, Radboud University Medical Center, Nijmegen, The Netherlands., Bollen S; Department of Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands., Elferink MG; Department of Genetics, University Medical Center Utrecht, Utrecht, The Netherlands., Straver R; Department of Clinical Genetics, VU University Medical Center, Amsterdam, The Netherlands., Henneman L; Department of Clinical Genetics, VU University Medical Center, Amsterdam, The Netherlands., Page-Christiaens GC; Department of Obstetrics and Gynaecology, University Medical Center Utrecht, Utrecht, The Netherlands., Sistermans EA; Department of Clinical Genetics, VU University Medical Center, Amsterdam, The Netherlands.
Publikováno v:
Genetics in medicine : official journal of the American College of Medical Genetics [Genet Med] 2018 Apr; Vol. 20 (5), pp. 480-485. Date of Electronic Publication: 2017 Sep 28.
Akademický článek
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Autor:
Jiang, Yan1 (AUTHOR), Xiao, Yang Xue1 (AUTHOR), Xiong, Jiao Jiao1 (AUTHOR), Zhang, Victor Wei2 (AUTHOR), Dong, Chang2 (AUTHOR), Xu, Lei2 (AUTHOR), Liu, Fang1 (AUTHOR) 23114271@qq.com
Publikováno v:
Molecular Cytogenetics (17558166). 1/3/2024, Vol. 17 Issue 1, p1-7. 7p.
Akademický článek
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Akademický článek
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