Zobrazeno 1 - 10
of 65
pro vyhledávání: '"Suijkerbuijk, Ron"'
Autor:
van Prooyen Schuurman, Lisanne, Sistermans, Erik A., Van Opstal, Diane, Henneman, Lidewij, Bekker, Mireille N., Bax, Caroline J., Pieters, Mijntje J., Bouman, Katelijne, de Munnik, Sonja, den Hollander, Nicolette S., Diderich, Karin E.M., Faas, Brigitte H.W., Feenstra, Ilse, Go, Attie T.J.I., Hoffer, Mariëtte J.V., Joosten, Marieke, Komdeur, Fenne L., Lichtenbelt, Klaske D., Lombardi, Maria P., Polak, Marike G., Jehee, Fernanda S., Schuring-Blom, Heleen, Stevens, Servi J.C., Srebniak, Malgorzata I., Suijkerbuijk, Ron F., Tan-Sindhunata, Gita M., van der Meij, Karuna R.M., van Maarle, Merel C., Vernimmen, Vivian, van Zelderen-Bhola, Shama L., van Ravesteyn, Nicolien T., Knapen, Maarten F.C.M., Macville, Merryn V.E., Galjaard, Robert-Jan H.
Publikováno v:
In The American Journal of Human Genetics 2 June 2022 109(6):1140-1152
Autor:
McGregor-Schuerman, Magda, Lo Fo Sang, Audrey, Bihari, Santusha, Ramdajal, Natasja, Suijkerbuijk, Ron F., van Ravenswaaij-Arts, Conny MA
Publikováno v:
In European Journal of Medical Genetics June 2020 63(6)
Akademický článek
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Akademický článek
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K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Galjaard, Robert-Jan, Henneman, Lidewij, Macville, Merryn, Bax, Caroline, Bekker, Mireille N., De Die-Smulders, Christine, Feenstra, Ilse, Hoffer, Mariette, Den Hollander, Nicolette, Knapen, Maarten F.C.M., Van Langen, Irene, Lichtenbelt, Klaske, Lombardi, Paola, Van Maarle, Merel, Van Der Meij, Karuna, Pieters, Mijntje, Schuring-Blom, Heleen, Sikkel, Esther, Stevens, Servi, Suijkerbuijk, Ron, Van Der Ven, Jeanine, Van Opstal, Diane, Weiss, Janneke, Sistermans, Erik
Publikováno v:
European Journal of Human Genetics, 27, 823-824. Nature Publishing Group
Weiss, M M, Galjaard, R H, Sistermans, E A, Bax, C J, Bekker, M N, de Die-Smulders, C E M, Feenstra, I, Hoffer, M J V, den Hollander, N S, Knapen, M F C M, van Langen, I M, Lichtenbelt, K D, Lombardi, P M, van Maarle, M C, van der Meij, K R M, Pieters, M J, Schuring-Blom, G H, Sikkel, E, Stevens, S J, Suijkerbuijk, R F, van der Ven, A J E M, Van Opstal, D, Henneman, L & Macville, M V 2019, ' Implementing NIPT as part of a national prenatal screening program: The Dutch TRIDENT studies ', European Journal of Human Genetics, vol. 27, pp. 823-824 .
Prenatal Diagnosis, 38(Suppl.1):2-3, 8-8. Wiley-Blackwell
Weiss, M M, Galjaard, R H, Sistermans, E A, Bax, C J, Bekker, M N, de Die-Smulders, C E M, Feenstra, I, Hoffer, M J V, den Hollander, N S, Knapen, M F C M, van Langen, I M, Lichtenbelt, K D, Lombardi, P M, van Maarle, M C, van der Meij, K R M, Pieters, M J, Schuring-Blom, G H, Sikkel, E, Stevens, S J, Suijkerbuijk, R F, van der Ven, A J E M, Van Opstal, D, Henneman, L & Macville, M V 2019, ' Implementing NIPT as part of a national prenatal screening program: The Dutch TRIDENT studies ', European Journal of Human Genetics, vol. 27, pp. 823-824 .
Prenatal Diagnosis, 38(Suppl.1):2-3, 8-8. Wiley-Blackwell
Objectives: In most countries, non-invasive prenatal testing (NIPT) has been introduced commercially without any governmental guidance. In the Netherlands, prenatal screening for fetal anomaly is subject to a governmental license. NIPT has been imple
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::17671380dcb3c74bfacb8ad89f8e02d1
https://research.vumc.nl/en/publications/896257aa-5289-4935-be6e-26f5fddee2d8
https://research.vumc.nl/en/publications/896257aa-5289-4935-be6e-26f5fddee2d8
Autor:
Galjaard, Robert-Jan, Henneman, Lidewij, Macville, Merryn, Bax, Caroline, Bekker, Mireille, De Die-Smulders, Christine, Feenstra, Ilse, Hoffer, Mariette, Den Hollander, Nicolette, Van Langen, Irene, Lichtenbelt, Klaske, Lombardi, Paola, Van Maarle, Merel, Van Der Meij, Karuna, Pieters, Mijntje, Schuring-Blom, Heleen, Sikkel, Esther, Stevens, Servi, Suijkerbuijk, Ron, Van Der Ven, Jeanine, Van Opstal, Diane, Weiss, Janneke, Sistermans, Erik
Publikováno v:
Prenatal Diagnosis, 38. John Wiley and Sons Ltd
Galjaard, R-J, Henneman, L, Macville, M, Bax, C, Bekker, M, De Die-Smulders, C, Feenstra, I, Hoffer, M, Den Hollander, N, Van Langen, I, Lichtenbelt, K, Lombardi, P, Van Maarle, M, Van Der Meij, K, Pieters, M, Schuring-Blom, H, Sikkel, E, Stevens, S, Suijkerbuijk, R, Van Der Ven, J, Van Opstal, D, Weiss, J & Sistermans, E 2018, ' Implementing NIPT as part of a national prenatal screening program: The Dutch TRIDENT studies ', Prenatal Diagnosis, vol. 38 .
Galjaard, R-J, Henneman, L, Macville, M, Bax, C, Bekker, M, De Die-Smulders, C, Feenstra, I, Hoffer, M, Den Hollander, N, Van Langen, I, Lichtenbelt, K, Lombardi, P, Van Maarle, M, Van Der Meij, K, Pieters, M, Schuring-Blom, H, Sikkel, E, Stevens, S, Suijkerbuijk, R, Van Der Ven, J, Van Opstal, D, Weiss, J & Sistermans, E 2018, ' Implementing NIPT as part of a national prenatal screening program: The Dutch TRIDENT studies ', Prenatal Diagnosis, vol. 38 .
Objectives: In most countries, non-invasive prenatal testing (NIPT) has been introduced commercially without any governmental guidance. In the Netherlands, prenatal screening for fetal anomaly is subject to a governmental license. NIPT has been imple
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::cb796c4d60389750bf9784f861377839
https://research.vumc.nl/en/publications/4d3b95e1-30fe-4485-ae05-ef25695b4f36
https://research.vumc.nl/en/publications/4d3b95e1-30fe-4485-ae05-ef25695b4f36
Autor:
Veltman, Imke *, van Asseldonk, Martien, Schepens, Marga, Stoop, Hans, Looijenga, Leendert, Wouters, Cokkie, Govaerts, Lutgarde, Suijkerbuijk, Ron, van Kessel, Ad Geurts
Publikováno v:
In Cancer Genetics and Cytogenetics 2002 136(1):17-22
Autor:
Bhola Shama L, Creemers Johan, Go Attie, Hoffer Mariëtte VJ, Huijsdens Karin, Kooper Angelique JA, Macville Merryn VE, Nijhuis Jan G, van Oppen Carla AC, Oepkes Dick, Schuring-Blom Heleen G, Wildschut Hajo I, Birnie Erwin, Boormans Elisabeth MA, Bilardo Katia M, Suijkerbuijk Ron, Bouman Katelijne, Galjaard Robert-Jan H, Bonsel Gouke J, van Lith Jan MM
Publikováno v:
BMC Pregnancy and Childbirth, Vol 8, Iss 1, p 18 (2008)
Abstract Background In the past 30 years karyotyping was the gold standard for prenatal diagnosis of chromosomal aberrations in the fetus. Traditional karyotyping (TKT) has a high accuracy and reliability. However, it is labor intensive, the results
Externí odkaz:
https://doaj.org/article/80c9712e3c424858b9c6b80a54bc59f0
Autor:
Bussey, Kimberly J, Lawce, Helen J, Himoe, Eleanor, Shu, Xiao Ou, Suijkerbuijk, Ron F, Olson, Susan B, Magenis, R.Ellen *
Publikováno v:
In Cancer Genetics and Cytogenetics 2001 125(2):112-118