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6 results for Die-Smulders,+Christine+EM+de

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Structural and functional cardiac changes in myotonic dystrophy type 1: a cardiovascular magnetic resonance study
Author / Creator:Hermans, Mieke CE ; Faber, Catharina G ; Bekkers, Sebastiaan CAM ; de Die-Smulders, Christine EM ; Gerrits, Monique M ; Merkies, Ingemar SJ ; Snoep, Gabriel ; Pinto, Yigal M ; Schalla, Simon
Publisher:England: BioMed Central Ltd
Journal title:Journal of cardiovascular magnetic resonance, 2012-07, Vol.14 (1), p.54-48, Article 54
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Advances in prenatal screening: the ethical dimension
Author / Creator:de Jong, Antina ; Dondorp, Wybo J. ; Frints, Suzanna G. M. ; de Die-Smulders, Christine E. M. ; de Wert, Guido M. W. R.
Publisher:London: Nature Publishing Group UK
Journal title:Nature reviews. Genetics, 2011-09, Vol.12 (9), p.657-663
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A comprehensive strategy for exome-based preconception carrier screening
Author / Creator:Sallevelt, Suzanne C.E.H. ; de Koning, Bart ; Szklarczyk, Radek ; Paulussen, Aimee D.C. ; de Die-Smulders, Christine E.M. ; Smeets, Hubert J.M.
Publisher:New York: Nature Publishing Group US
Journal title:Genetics in medicine, 2017-05, Vol.19 (5), p.583-592
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Preimplantation genetic diagnosis (PGD) for Huntington's disease: the experience of three European centres
Author / Creator:Van Rij, Maartje C ; De Rademaeker, Marjan ; Moutou, Céline ; Dreesen, Jos CFM ; De Rycke, Martine ; Liebaers, Inge ; Geraedts, Joep PM ; De Die-Smulders, Christine EM ; Viville, Stéphane
Publisher:Basingstoke: Nature Publishing Group
Journal title:European journal of human genetics : EJHG, 2012-04, Vol.20 (4), p.368-375
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SNP array-based copy number and genotype analyses for preimplantation genetic diagnosis of human unbalanced translocations
Author / Creator:van Uum, Chris MJ ; Stevens, Servi JC ; Dreesen, Joseph CFM ; Drüsedau, Marion ; Smeets, Hubert J ; Hollanders-Crombach, Bertien ; Die-Smulders, Christine EM de ; Geraedts, Joep PM ; Engelen, John JM ; Coonen, Edith
Publisher:Basingstoke: Nature Publishing Group
Journal title:European journal of human genetics : EJHG, 2012-09, Vol.20 (9), p.938-944
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Analysis of severely affected patients with dihydropyrimidine dehydrogenase deficiency reveals large intragenic rearrangements of DPYD and a de novo interstitial deletion del(1)(p13.3p21.3)
Author / Creator:van Kuilenburg, André B. P ; Meijer, Judith ; Mul, Adri N. P. M ; Hennekam, Raoul C. M ; Hoovers, Jan M. N ; de Die-Smulders, Christine E. M ; Weber, Peter ; Mori, Andrea Capone ; Bierau, Jörgen ; Fowler, Brian ; Macke, Klaus ; Sass, Jörn Oliver ; Meinsma, Rutger ; Hennermann, Julia B ; Miny, Peter ; Zoetekouw, Lida ; Vijzelaar, Raymon ; Nicolai, Joost ; Ylstra, Bauke ; Rubio-Gozalbo, M. Estela
Publisher:Berlin/Heidelberg: Berlin/Heidelberg : Springer-Verlag
Journal title:Human genetics, 2009-06, Vol.125 (5-6), p.581-590
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Structural and functional cardiac changes in myotonic dystrophy type 1: a cardiovascular magnetic resonance study

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Advances in prenatal screening: the ethical dimension

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A comprehensive strategy for exome-based preconception carrier screening

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Preimplantation genetic diagnosis (PGD) for Huntington's disease: the experience of three European centres

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SNP array-based copy number and genotype analyses for preimplantation genetic diagnosis of human unbalanced translocations

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Analysis of severely affected patients with dihydropyrimidine dehydrogenase deficiency reveals large intragenic rearrangements of DPYD and a de novo interstitial deletion del(1)(p13.3p21.3)

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