Selective chromosome analysis in couples with two or more miscarriages: case-control study
Franssen, Maureen T M, Korevaar, Johanna C, Leschot, Nico J, Bossuyt, Patrick M M, Knegt, Alida C, Gerssen-Schoorl, Klasien B J, Wouters, Cokkie H, Hansson, Kerstin B M, Hochstenbach, Ron, Madan, Kamlesh, van der Veen, Fulco, Goddijn, Mariette
Published in BMJ (16.07.2005)
Published in BMJ (16.07.2005)
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Ring chromosome formation as a novel escape mechanism in patients with inverted duplication and terminal deletion
KNIJNENBURG, Jeroen, VAN HAERINGEN, Arie, HANSSON, Kerstin B. M, LANKESTER, Arjan, SMIT, Margot J. M, BELFROID, René D. M, BAKKER, Egbert, ROSENBERG, Carla, TANKE, Hans J, SZUHAI, Karoly
Published in European journal of human genetics : EJHG (01.05.2007)
Published in European journal of human genetics : EJHG (01.05.2007)
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The clinical spectrum of complete FBN1 allele deletions
HILHORST-HOFSTEE, Yvonne, HAMEL, Ben Cj, MOLL, Henriette A, BREUNING, Martijn H, PALS, Gerard, VERHEIJ, Joke Bgm, RIJLAARSDAM, Marry Eb, MANCINI, Grazia Ms, COBBEN, Jan M, GIROTH, Cindy, RUIVENKAMP, Claudia Al, HANSSON, Kerstin Bm, TIMMERMANS, Janneke
Published in European journal of human genetics : EJHG (01.03.2011)
Published in European journal of human genetics : EJHG (01.03.2011)
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Low uptake of prenatal diagnosis after established carrier status of a balanced structural chromosome abnormality in couples with recurrent miscarriage
Vansenne, Fleur, M.D, de Borgie, Corianne A.J.M., M.D., Ph.D, Korevaar, Johanna C., Ph.D, Franssen, Maureen T.M., M.D, Pajkrt, Eva, M.D., Ph.D, Hansson, Kerstin B.M., Ph.D, Leschot, Nico J., M.D., Ph.D, Bossuyt, Patrick M.M., M.D., Ph.D, van der Veen, Fulco, M.D., Ph.D, Goddijn, Mariëtte, M.D., Ph.D
Published in Fertility and sterility (01.06.2010)
Published in Fertility and sterility (01.06.2010)
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Quantification of sequence exchange events between PMS2 and PMS2CL provides a basis for improved mutation scanning of lynch syndrome patients
van der Klift, Heleen M, Tops, Carli M.J, Bik, Elsa C, Boogaard, Merel W, Borgstein, Anne-Marijke, Hansson, Kerstin B.M, Ausems, Margreet G.E.M, Garcia, Encarna Gomez, Green, Andrew, Hes, Frederik J, Izatt, Louise, van Hest, Liselotte P, Alonso, Angel M, Vriends, Annette H.J.T, Wagner, Anja, van Zelst-Stams, Wendy A.G, Vasen, Hans F.A, Morreau, Hans, Devilee, Peter, Wijnen, Juul T
Published in Human mutation (01.05.2010)
Published in Human mutation (01.05.2010)
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Molecular and clinical characterization of patients with a ring chromosome 11
Hansson, Kerstin B.M, Gijsbers, Antoinet C.J, Oostdijk, Wilma, Rehbock, Jan J.B, de Snoo, Femke, Ruivenkamp, Claudia A.L, Kant, Sarina G
Published in European journal of medical genetics (01.12.2012)
Published in European journal of medical genetics (01.12.2012)
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Three new cases with a mosaicism involving a normal cell line and a cryptic unbalanced autosomal reciprocal translocation
Gijsbers, Antoinet C.J, Dauwerse, Johannes G, Bosch, Cathy A.J, Boon, Elles M.J, van den Ende, Wilco, Kant, Sarina G, Hansson, Kerstin M.B, Breuning, Martijn H, Bakker, Egbert, Ruivenkamp, Claudia A.L
Published in European journal of medical genetics (01.07.2011)
Published in European journal of medical genetics (01.07.2011)
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Mutations in DNMT3B Modify Epigenetic Repression of the D4Z4 Repeat and the Penetrance of Facioscapulohumeral Dystrophy
van den Boogaard, Marlinde L., Lemmers, Richard J.L.F., Balog, Judit, Wohlgemuth, Mariëlle, Auranen, Mari, Mitsuhashi, Satomi, van der Vliet, Patrick J., Straasheijm, Kirsten R., van den Akker, Rob F.P., Kriek, Marjolein, Laurense-Bik, Marlies E.Y., Raz, Vered, van Ostaijen-ten Dam, Monique M., Hansson, Kerstin B.M., van der Kooi, Elly L., Kiuru-Enari, Sari, Udd, Bjarne, van Tol, Maarten J.D., Nishino, Ichizo, Tawil, Rabi, Tapscott, Stephen J., van Engelen, Baziel G.M., van der Maarel, Silvère M.
Published in American journal of human genetics (05.05.2016)
Published in American journal of human genetics (05.05.2016)
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