Search Results - Hansson, Kerstin B.M

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  1. 1
    Mutations in DNMT3B Modify Epigenetic Repression of the D4Z4 Repeat and the Penetrance of Facioscapulohumeral Dystrophy

    Mutations in DNMT3B Modify Epigenetic Repression of the D4Z4 Repeat and the Penetrance of Facioscapulohumeral Dystrophy by 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.

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  2. 2
    Molecular and clinical characterization of patients with a ring chromosome 11

    Molecular and clinical characterization of patients with a ring chromosome 11 by Hansson, Kerstin B.M, Gijsbers, Antoinet C.J, Oostdijk, Wilma, Rehbock, Jan J.B, de Snoo, Femke, Ruivenkamp, Claudia A.L, Kant, Sarina G

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  3. 3
    The clinical spectrum of complete FBN1 allele deletions

    The clinical spectrum of complete FBN1 allele deletions by Hilhorst-Hofstee, Yvonne, Hamel, Ben CJ, Verheij, Joke BGM, Rijlaarsdam, Marry EB, Mancini, Grazia MS, Cobben, Jan M, Giroth, Cindy, Ruivenkamp, Claudia AL, Hansson, Kerstin BM, Timmermans, Janneke, Moll, Henriette A, Breuning, Martijn H, Pals, Gerard

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  4. 4
    Selective chromosome analysis in couples with two or more miscarriages: case-control study

    Selective chromosome analysis in couples with two or more miscarriages: case-control study by 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
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  5. 5
    Interstitial deletion of 6q without phenotypic effect

    Interstitial deletion of 6q without phenotypic effect by Hansson, Kerstin, Szuhai, Karoly, Knijnenburg, Jeroen, van Haeringen, Arie, de Pater, Joke

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  6. 6
    The clinical spectrum of complete allele deletions

    The clinical spectrum of complete allele deletions by Hilhorst-Hofstee, Yvonne, Hamel, Ben Jc, Verheij, Joke B.G.M., Rijlaarsdam, Marry Eb, Mancini, Grazia Ms, Cobben, Jan Maarten, Giroth, Cindy, Ruivenkamp, Claudia, Hansson, Kerstin B.M., Timmermans, Janneke, Moll, Henriette, Breuning, Martijn H., Pals, Gerard

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