CNTNAP2 gene dosage variation is associated with schizophrenia and epilepsy von Friedman, J I, Vrijenhoek, T, Markx, S, Janssen, I M, van der Vliet, W A, Faas, B H W, Knoers, N V, Cahn, W, Kahn, R S, Edelmann, L, Davis, K L, Silverman, J M, Brunner, H G, van Kessel, A Geurts, Wijmenga, C, Ophoff, R A, Veltman, J A

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Identification of clinically significant, submicroscopic chromosome alterations and UPD in fetuses with ultrasound anomalies using genome-wide 250k SNP array analysis von Faas, B H W, van der Burgt, I, Kooper, A J A, Pfundt, R, Hehir-Kwa, J Y, Smits, A P T, de Leeuw, N

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Clinical utility of non‐invasive prenatal testing in pregnancies with ultrasound anomalies von Beulen, L., Faas, B. H. W., Feenstra, I., van Vugt, J. M. G., Bekker, M. N.

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SNP Array Analysis in Constitutional and Cancer Genome Diagnostics – Copy Number Variants, Genotyping and Quality Control von de Leeuw, N., Hehir-Kwa, J.Y., Simons, A., Geurts van Kessel, A., Smeets, D.F., Faas, B.H.W., Pfundt, R.

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Detection of fetal RHD-specific sequences in maternal plasma von Faas, BHW, Beuling, EA, Christiaens, GC ML, von dem Borne, AEG Kr, van der School, CE

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Erratum: CNTNAP2 gene dosage variation is associated with schizophrenia and epilepsy von Friedman, J I, Vrijenhoek, T, Markx, S, Janssen, I M, van der Vliet, W A, Faas, B H W, Knoers, N V, Cahn, W, Kahn, R S, Edelmann, L, Davis, K L, Silverman, J M, Brunner, H G, Geurts van Kessel, A, Wijmenga, C, Ophoff, R A, Veltman, J A

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CNTNAP2 gene dosage variation is associated with schizophrenia and epilepsy von Friedman, J I, Vrijenhoek, T, Markx, S, Janssen, I M, Van Der Vliet, W A, Faas, B H W, Knoers, N V, Cahn, W, Kahn, R S, Edelmann, L, Davis, K L, Silverman, J M, Brunner, H G, Geurts Van Kessel, A, Wijmenga, C, Ophoff, R A, Veltman, J A

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A new case of dup(3q) syndrome due to a pure duplication of 3qter von Faas, BHW, De Vries, BBA, Van Es-van Gaal, J, Merkx, G, Draaisma, JMT, Smeets, DFCM

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Clinical Utility of Noninvasive Prenatal Testing in Pregnancies With Ultrasound Anomalies von Beulen, L., Faas, B. H. W., Feenstra, I., Van Vugt, J. M. G., Bekker, M. N.

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Prenatal cell-free DNA testing of women with pregnancy-associated cancer: a retrospective cross-sectional study von Heesterbeek, Catharina J., Tjan-Heijnen, Vivianne C.G., Heimovaara, Joosje H., Lenaerts, Liesbeth, Lok, Christianne, Vriens, Ingeborg J.H., Van Opstal, Diane, Boon, Elles M.J., Sie, Daoud, de Die-Smulders, Christine E.M., Amant, Frédéric, Macville, Merryn V.E., Sistermans, E.A., Henneman, L., Polstra, A., Voorhoeve, E., Zelderen-Bohla, S.L., Boon, E.M.J., Lombardi, M.P.R., Louwerens-Zintel, C., Smit, M., van Maarle, M.C., Tan-Sindhunata, M.B., van der Meij, K., Meij, H., Bax, C., Pajkrt, E., Linskens, I.H., Martin, L., Gitsels-van der Wal, J.T., Galjaard, R.J.H., Van Opstal, D., Srebniak, M.I., Jehee, F.M. Sarquis, Hollink, I.H.I.M., Sleutels, F., de Valk, W., Deelen, W.H., Joosten, A.M.S., Diderich, K.E.M., Redeker, M.E., Go, A.T.J.I., Knapen, M.F.C.M., Galjaard, S., Prinsen, A.K.E., Braat, A.P.G., Macville, M.V.E., Stevens, S.J.C., van der Wijngaard, A., Houben, L.H., van Esch-Lennarts, M.A.A., Hamers, L., Jetten, A.G.P., Ghesquiere, S.A.I., Koning, B. de, ZamaniEsteki, M., Heesterbeek, C.J., de Die-Smulders, C.E.M., Brunner, H., Pieters, M.J., Coumans, A.B.C., Smeets, D.F.C.M., Faas, B.H.W., Westra, D., Weiss, M.M., Derks-Prinsen, I., Feenstra, I., van Rij, M., Sikkel, E., Hoffer, M.J.V., Hollander, N.S. den, Verweij, E.J.T., Haak, M.C., Suijkerbuijk, R.F., Sikkema-Raddatz, B., van Langen, I.M., Bouman, K., Duin, L.K., Schuring-Blom, G.H., Lichtenbelt, K.D., Bekker, M.N., van der Ven, A.J.E.M., van Vliet-Lachotzki, E., Pot, J., van ‘t Padje, S., Bakker, I.M.C., Bradley, E.J.

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The VS and V blood group polymorphisms in Africans: a serologic and molecular analysis von Daniels, G. L., Faas, B.H.W., Green, C. A., Smart, E., Maaskant-van Wijk, P. A., Avent, N. D., Zondervan, H. A., von dem Borne, A. E., van der Schoot, C. E.

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Molecular background of VS and weak C expression in blacks von Faas, B.H.W., Beckers, E.A.M., Wildoer, P., Ligthart, P.C., Overbeeke, M.A.M., Zondervan, H.A., von dem Borne, A.E.G.Kr, van der Schoot, C.E.

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Genotyping of RHD by multiplex polymerase chain reaction analysis of six RHD-specific exons von Maaskant-van Wijk, P. A., Faas, B.H.W., de Ruijter, J.A.M., Overbeeke, M.A.M., von dem Borne, A.E.G.Kr, van Rhenen, D. J., van der Schoot, C. E.

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Rapid Rh D Genotyping by Polymerase Chain Reaction-Based Amplification of DNA von Simsek, S., Faas, B.H.W., Bleeker, P.M.M., Overbeeke, M.A.M., Cuijpers, H.Th.M., van der Schoot, C.E., von dem Borne, A.E.G.Kr

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Rh E/e Genotyping by Allele-Specific Primer Amplification von Faas, B.H.W., Simsek, S., Bleeker, P.M.M., Overbeeke, M.A.M., Cuijpers, H.Th.M., Borne, A.E.G.Kr. von dem, Schoot, C.E. van der

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Involvement of Gly96 in the formation of the Rh26 epitope von Faas, B.H.W, Ligthart, P.C., Lomas-Francis, C., Overbeeke, M.A.M., von dem Borne, A.E.G., van der Schoot, C.E.

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Lower antigen site density and weak D immunogenicity cannot be explained by structural genomic abnormalities or regulatory defects of the RHD gene von Beckers, E.A.M., Faas, B.H.W., Ligthart, P., Overbeeke, M.A.M., von dem Borne, A.E.G., van der Schoot, C.E., van Rhenen, D.J.

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The applicability of different PCR-based methods for fetal RHD and K1 genotyping: a prospective study von Faas, B. H. W., Maaskant-van Wijk, P. A., von dem Borne, A. E. G. Kr, van der Schoot, C. E., Christiaens, G. C. M. L.

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The applicability of different PCR-based methods for fetalRHD andK1 genotyping: a prospective study von Faas, B. H. W., Maaskant-van Wijk, P. A., von dem Borne, A. E. G. Kr, van der Schoot, C. E., Christiaens, G. C. M. L.

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Rh DNA analysis von Maaskant-van Wijk, P.A., Faas, B.H.W., Wildoer, P., Ligthart, P.C., Overbeeke, M.A.M., Kr. von dem Borne, A.E.G., Van Rhenen, D.J., Van der Schoot, C.E.

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