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11دورية أكاديمية
المؤلفون: de Leeuw, B, Berger, W, Sinke, R, Suijkerbuijk, R, Gilgenkrantz, S, Geraghty, M, Valle, D, Monaco, A, Lehrach, H, Ropers, H
العلاقة: https://ora.ox.ac.uk/objects/uuid:7a9bba2f-0273-4205-9b27-33078f06d582Test; https://doi.org/10.1002/gcc.2870060309Test
الإتاحة: https://doi.org/10.1002/gcc.2870060309Test
https://ora.ox.ac.uk/objects/uuid:7a9bba2f-0273-4205-9b27-33078f06d582Test -
12دورية أكاديمية
المؤلفون: Suijkerbuijk, R, Meloni, A, Sinke, R, de Leeuw, B, Wilbrink, M, Janssen, H, Geraghty, M, Monaco, A, Sandberg, A, Geurts van Kessel, A
العلاقة: https://ora.ox.ac.uk/objects/uuid:5e848741-e953-4f19-9a08-92c4dc790e21Test; https://doi.org/10.1016/0165-4608Test(93)90024-g
الإتاحة: https://doi.org/10.1016/0165-4608Test(93)90024-g
https://ora.ox.ac.uk/objects/uuid:5e848741-e953-4f19-9a08-92c4dc790e21Test -
13دورية أكاديمية
المؤلفون: Van Echten-Arends, J., Coonen, E., Reuters, B., Suijkerbuijk, R. F., Dul, E. C., Land, J. A., van Ravenswaaij-Arts, C. M. A.
المصدر: Van Echten-Arends , J , Coonen , E , Reuters , B , Suijkerbuijk , R F , Dul , E C , Land , J A & van Ravenswaaij-Arts , C M A 2013 , ' Preimplantation genetic diagnosis for X;autosome translocations : lessons from a case of misdiagnosis ' , Human Reproduction , vol. 28 , no. 11 , pp. 3141-3145 . https://doi.org/10.1093/humrep/det362Test ; ISSN:0268-1161
مصطلحات موضوعية: PGD, misdiagnosis, reciprocal translocation, X-autosome translocation, segregation types, IN-SITU HYBRIDIZATION, ESHRE PGD CONSORTIUM, RECIPROCAL TRANSLOCATIONS, PRACTICE GUIDELINES, SEGREGATION MODES, NEWBORNS, CARRIERS, OUTCOMES, EMBRYOS, envir, socio
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14دورية أكاديمية
المؤلفون: van der Kevie-Kersemaekers, A. M. F., Suijkerbuijk, R. F., Moll, F. C. P., Dijkhuizen, T., van Spaendonck-Zwarts, K. Y., Drok, G., Bouman, K., Sikkema-Raddatz, B.
المصدر: van der Kevie-Kersemaekers , A M F , Suijkerbuijk , R F , Moll , F C P , Dijkhuizen , T , van Spaendonck-Zwarts , K Y , Drok , G , Bouman , K & Sikkema-Raddatz , B 2010 , ' A live-born child with a mosaic chromosomal pattern of either monosomy 21 or trisomy 4 in different embryonal germ layers ' , Prenatal Diagnosis , vol. 30 , no. 1 , pp. 86-88 . https://doi.org/10.1002/pd.2415Test
مصطلحات موضوعية: prenatal, monosomy 21, trisomy 4, mosaicism, embryonal germ layers, DIAGNOSIS
الإتاحة: https://doi.org/10.1002/pd.2415Test
https://hdl.handle.net/11370/0b0d4b02-e79e-46c8-858c-0b328cfe7f6dTest
https://research.rug.nl/en/publications/0b0d4b02-e79e-46c8-858c-0b328cfe7f6dTest -
15دورية أكاديمية
المؤلفون: Sikkema-Raddatz, B., Bouman, K., Drok, G., ter Brugge, H. G., Suijkerbuijk, R.
المصدر: Sikkema-Raddatz , B , Bouman , K , Drok , G , ter Brugge , H G & Suijkerbuijk , R 2009 , ' A non-mosaic tetraploidy in the long-term culture of chorionic villi with a trisomy 13 in concomitant amniocytes ' , Prenatal Diagnosis , vol. 29 , no. 5 , pp. 541-542 . https://doi.org/10.1002/pd.2226Test
مصطلحات موضوعية: trisomy 13, tetraploidy, potentially false-negative, mosaicism, PRENATAL-DIAGNOSIS, FETUS, CVS
الإتاحة: https://doi.org/10.1002/pd.2226Test
https://hdl.handle.net/11370/4928fb90-ba52-4542-99db-c0012cc23809Test
https://research.rug.nl/en/publications/4928fb90-ba52-4542-99db-c0012cc23809Test -
16دورية أكاديمية
المؤلفون: van der Kevie‐Kersemaekers, A. M. F., Suijkerbuijk, R. F., Moll, F. C. P., Dijkhuizen, T., van Spaendonck‐Zwarts, K. Y., Drok, G., Bouman, K., Sikkema‐Raddatz, B.
المصدر: Prenatal Diagnosis ; volume 30, issue 1, page 86-88 ; ISSN 0197-3851 1097-0223
الإتاحة: https://doi.org/10.1002/pd.2415Test
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17كتاب
المؤلفون: Suijkerbuijk, R. F., Sinke, R. J., Looijenga, L. H. J., de Jong, B., Oosterhuis, J. W., Cassiman, J. J., van Kessel, A. Geurts
المصدر: Chromosome 12 Aberrations in Human Solid Tumors ; page 124-137 ; ISBN 9783662062579 9783662062555
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18دورية أكاديمية
المؤلفون: Veltman, I, van Asseldonk, M, Schepens, M, Stoop, Hans, Looijenga, LHJ (Leendert), Wouters, Cokkie, Govaerts, LCP, Suijkerbuijk, R, van Kessel, AG
المصدر: Veltman , I , van Asseldonk , M , Schepens , M , Stoop , H , Looijenga , LHJ , Wouters , C , Govaerts , LCP , Suijkerbuijk , R & van Kessel , AG 2002 , ' A novel case of infantile sacral teratoma and a constitutional t(12;15)(q13;q25) pat ' , Cancer Genetics & Cytogenetics , vol. 136 , pp. 17-22 . https://doi.org/10.1016/S0165-4608Test(01)00666-5
مصطلحات موضوعية: /dk/atira/pure/keywords/researchprograms/AFL001000/EMCMGC029601, name=EMC MGC-02-96-01, /dk/atira/pure/keywords/researchprograms/AFL001000/EMCMM032407, name=EMC MM-03-24-07
الإتاحة: https://doi.org/10.1016/S0165-4608Test(01)00666-5
https://pure.eur.nl/en/publications/e80d803e-bbff-425e-b326-c53189b0bdf0Test
http://hdl.handle.net/1765/58514Test -
19كتاب
المصدر: Pathobiology of Human Germ Cell Neoplasia ; Recent Results in Cancer Research ; page 113-118 ; ISSN 0080-0015 ; ISBN 9783642844874 9783642844850
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20دورية أكاديمية
المؤلفون: Simons, Annet, Schepens, M, Jeuken, J, Sprenger, S., van de Zande, G, Bjerkehagen, B, Forus, A, Weibolt, V., Molenaar, Ineke, van den Berg-de Ruiter, Eva, Myklebost, O, Bridge, J, Geurts van Kessel, A., Suijkerbuijk, R
المصدر: Simons , A , Schepens , M , Jeuken , J , Sprenger , S , van de Zande , G , Bjerkehagen , B , Forus , A , Weibolt , V , Molenaar , I , van den Berg-de Ruiter , E , Myklebost , O , Bridge , J , Geurts van Kessel , A & Suijkerbuijk , R 2000 , ' Frequent loss of 9p21 (p16(INK4A)) and other genomic imbalances in human malignant fibrous histiocytoma ' , Cancer Genetics and Cytogenetics , vol. 118 , no. 2 , pp. 89-98 .
مصطلحات موضوعية: SOFT-TISSUE SARCOMAS, 19P+ MARKER CHROMOSOME, RETINOBLASTOMA GENE, PROSTATE-CANCER, SOLID TUMORS, HYBRIDIZATION, AMPLIFICATION, AMPLICON, BONE, IDENTIFICATION