Best diagnostic approach for the genetic evaluation of fetuses after intrauterine death in first, second or third trimester: QF-PCR, karyotyping and/or genome wide SNP array analys...

Por Kooper, Angelique JA, Faas, Brigitte HW, Feenstra, Ilse, de Leeuw, Nicole, Smeets, Dominique FCM
Publicado em 2014

Is routine karyotyping required in prenatal samples with a molecular or metabolic referral?

Por Kooper, Angelique JA, Pieters, Jacqueline JPM, Faas, Brigitte HW, Hoefsloot, Lies H, van der Burgt, Ineke, Zondervan, Hans A, Smits, Arie PT
Publicado em 2012

Detection of Chromosome Aneuploidies in Chorionic Villus Samples by Multiplex Ligation-Dependent Probe Amplification

Por Kooper, Angelique J.A., Faas, Brigitte H.W., Feuth, Ton, Creemers, Johan W.T., Zondervan, Hans H., Boekkooi, Peter F., Quartero, Rik W.P., Rijnders, Robbert J.P., van der Burgt, Ineke, van Kessel, Ad Geurts, Smits, Arie P.T.
Publicado em 2009

Multiplex ligation-dependent probe amplification versus karyotyping in prenatal diagnosis: the M.A.K.E. study

Por Boormans, Elisabeth MA, Birnie, Erwin, Wildschut, Hajo I, Schuring-Blom, Heleen G, Oepkes, Dick, van Oppen, Carla AC, Nijhuis, Jan G, Macville, Merryn VE, Kooper, Angelique JA, Huijsdens, Karin, Hoffer, Mariëtte VJ, Go, Attie, Creemers, Johan, Bhola, Shama L, Bilardo, Katia M, Suijkerbuijk, Ron, Bouman, Katelijne, Galjaard, Robert-Jan H, Bonsel, Gouke J, van Lith, Jan MM
Publicado em 2008