المؤلفون: De Krom, G., Severijns, Y., Vlieg, W. L., Arens, Y. H. J. M., Van Golde, R. J. T., De Die-Smulders, C. E. M., Van Osch, L. A. D. M.

المساهمون: ZonMW

المصدر: Journal of Assisted Reproduction and Genetics ; volume 37, issue 7, page 1719-1727 ; ISSN 1058-0468 1573-7330

مصطلحات موضوعية: Genetics (clinical), Developmental Biology, Obstetrics and Gynecology, Genetics, Reproductive Medicine, General Medicine

الإتاحة: https://doi.org/10.1007/s10815-020-01810-wTest

المؤلفون: van Rijsingen, I. A. W., Bekkers, S. C. A. M., Schalla, S., Hermans-van Ast, J. F., Snoep, G., Alzand, B. S. N., Arens, Y. H. J. M., van den Wijngaard, A., Crijns, H. J. G. M., Pinto, Y. M.

المصدر: Netherlands Heart Journal ; volume 19, issue 4, page 168-174 ; ISSN 1568-5888 1876-6250

مصطلحات موضوعية: Cardiology and Cardiovascular Medicine

الإتاحة: https://doi.org/10.1007/s12471-011-0090-8Test

المؤلفون: Christiaans, I., Birnie, E., Bonsel, G. J., Mannens, M. M. A. M., Michels, M., Majoor-Krakauer, D., Dooijes, D., van Tintelen, J. P., van den Berg, M. P., Volders, P. G. A., Arens, Y. H., van den Wijngaard, A., Atsma, D. E., Helderman-van den Enden, A. T. J. M., Houweling, A. C., de Boer, K., van der Smagt, J. J., Hauer, R. N. W., Marcelis, C. L. M., Timmermans, J., van Langen, I. M., Wilde, A. A. M.

المصدر: European Heart Journal ; volume 32, issue 9, page 1161-1170 ; ISSN 0195-668X 1522-9645

الإتاحة: https://doi.org/10.1093/eurheartj/ehr092Test
http://academic.oup.com/eurheartj/article-pdf/32/9/1161/1562099/ehr092.pdfTest

المؤلفون: Paulussen, A DC, Schrander-Stumpel, Connie, Tserpelis, D, Spee, K, Stegmann, Sander, Mancini, Grazia Maria Stefania, Brooks, Alice S, Collée, J M, Maat-Kievit, Anneke, Simon, M EH, Van Bever, Yolande, Stolte-Dijkstra, Irene, Kerstjens-Frederikse, W S, Herkert, J C, Van Essen, Ton J., Lichtenbelt, K D, Van Haeringen, Arie, Kwee, Mei Lan, Lachmeijer, A. M.A., Tan-Sindhunata, M.B., Van Maarle, Merel, Arens, Y H, Smeets, Eric, De Die-Smulders, Christine E.M., Engelen, John J, Smeets, Bert, Herbergs, J

المساهمون: Department of Clinical Genetics

المصدر: ISSN: 1018-4813.

مصطلحات موضوعية: Holoprosencephaly, genotype-phenotype, mutations

العلاقة: hal-00544822; https://hal.archives-ouvertes.fr/hal-00544822Test; https://hal.archives-ouvertes.fr/hal-00544822/documentTest; https://hal.archives-ouvertes.fr/hal-00544822/file/PEER_stage2_10.1038%252Fejhg.2010.70.pdfTest

الإتاحة: https://doi.org/10.1038/ejhg.2010.70Test
https://hal.archives-ouvertes.fr/hal-00544822Test
https://hal.archives-ouvertes.fr/hal-00544822/documentTest
https://hal.archives-ouvertes.fr/hal-00544822/file/PEER_stage2_10.1038%252Fejhg.2010.70.pdfTest

المؤلفون: De Krom, G., Arens, Y. H J M, Coonen, E., Van Ravenswaaij-Arts, C. M A, Meijer-Hoogeveen, M., Evers, J. L H, van Golde, Ron J T, de Die-Smulders, Christine E M

المساهمون: Fertiliteitartsen, Child Health

مصطلحات موضوعية: Genetic counselling, PGD, Recurrent miscarriage, Reproductive decision-making, Structural chromosomal abnormalities, Reproductive Medicine, Rehabilitation, Obstetrics and Gynaecology

وصف الملف: application/pdf

العلاقة: https://dspace.library.uu.nl/handle/1874/357628Test

الإتاحة: https://dspace.library.uu.nl/handle/1874/357628Test

المؤلفون: De Krom, G., Arens, Y. H. J. M., Coonen, E., Van Ravenswaaij-Arts, C. M. A., Meijer-Hoogeveen, M., Evers, J. L. H., Van Golde, R. J. T., De Die-Smulders, C. E. M.

المصدر: De Krom , G , Arens , Y H J M , Coonen , E , Van Ravenswaaij-Arts , C M A , Meijer-Hoogeveen , M , Evers , J L H , Van Golde , R J T & De Die-Smulders , C E M 2015 , ' Recurrent miscarriage in translocation carriers : no differences in clinical characteristics between couples who accept and couples who decline PGD ' , Human Reproduction , vol. 30 , no. 2 , pp. 484-489 . https://doi.org/10.1093/humrep/deu314Test

مصطلحات موضوعية: genetic counselling, PGD, structural chromosomal abnormalities, recurrent miscarriage, reproductive decision-making, PREIMPLANTATION GENETIC DIAGNOSIS, CHROMOSOME ANALYSIS, RISK

العلاقة: https://research.rug.nl/en/publications/0c472730-f3be-4cbe-90bf-1594661bd520Test

الإتاحة: https://doi.org/10.1093/humrep/deu314Test
https://hdl.handle.net/11370/0c472730-f3be-4cbe-90bf-1594661bd520Test
https://research.rug.nl/en/publications/0c472730-f3be-4cbe-90bf-1594661bd520Test

المؤلفون: van Rijsingen, I. A. W., Ast, J. F. Hermans-van, Arens, Y. H. J. M., Schalla, S. M., de Die-Smulders, C. E. M, van den Wijngaard, A., Pinto, Y. M.

المصدر: Netherlands Heart Journal ; volume 17, issue 12, page 458-463 ; ISSN 1568-5888 1876-6250

مصطلحات موضوعية: Cardiology and Cardiovascular Medicine

الإتاحة: https://doi.org/10.1007/bf03086304Test

المؤلفون: Moog, U.^1,2 ute.moog@gen.unimaas.nl, Arens, Y. H. J. M.¹, van Lent-Albrechts, J. C. M.¹, Huijts, P. E. A.¹, Smeets, E. E. J.¹, Schrander-Stumpel, C. T. R. M.^1,2, Engelen, J. J. M.^1,2

المصدر: Clinical Genetics. Nov2005, Vol. 68 Issue 5, p397-407. 11p. 2 Black and White Photographs, 1 Chart.

مصطلحات موضوعية: *CHROMOSOMES, *GENES, *MEDICAL genetics, *HUMAN genetics, *INTELLECTUAL disabilities, *DEVELOPMENTAL disabilities

المؤلفون: Kleefstra, T., Franken, C. E., Arens, Y. H. J. M., Ramakers, G. J. A., Yntema, H. G., Sistermans, E. A., Hulsmans, C. F. C. H., Nillesen, W. N., van Bokhoven, H., de Vries, B. B. A., Hamel, B. C. J.

المصدر: Clinical Genetics; Oct2004, Vol. 66 Issue 4, p318-326, 9p

مصطلحات موضوعية: CARRIER proteins, GENES, INTELLECTUAL disabilities, PHENOTYPES, GENETICS, GENETIC mutation