Search Results - Vermeulen, Sita H.H.M.

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  1. 1
    Polymorphisms in the H19 Gene and the Risk of Bladder Cancer

    Polymorphisms in the H19 Gene and the Risk of Bladder Cancer by Verhaegh, Gerald W, Verkleij, Linda, Vermeulen, Sita H.H.M, den Heijer, Martin, Witjes, J. Alfred, Kiemeney, Lambertus A

    Published in European urology
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  2. 2
    Maternal MTHFR 677C>T is a risk factor for congenital heart defects: effect modification by periconceptional folate supplementation

    Maternal MTHFR 677C>T is a risk factor for congenital heart defects: effect modification by periconceptional folate supplementation by van Beynum, Ingrid M., Kapusta, Livia, den Heijer, Martin, Vermeulen, Sita H.H.M., Kouwenberg, Margreet, Daniëls, Otto, Blom, Henk J.

    Published in European heart journal
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  3. 3
    Smoking intensity and bladder cancer aggressiveness at diagnosis

    Smoking intensity and bladder cancer aggressiveness at diagnosis by Barbosa, André L A, Vermeulen, Sita H H M, Aben, Katja K, Grotenhuis, Anne J, Vrieling, Alina, Kiemeney, Lambertus A

    Published in PloS one
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  4. 4
    Genetics of hypospadias: are single nucleotide polymorphisms in srd5a2, esr1, esr2 and atf3 really associated with the malformation?

    Genetics of hypospadias: are single nucleotide polymorphisms in srd5a2, esr1, esr2 and atf3 really associated with the malformation? by Van Der Zanden, Loes F.M, Van Rooij, Iris A.L.M, Feitz, Wout F.J, Vermeulen, Sita H.H.M, Kiemeney, Lambertus A.L.M, Knoers, Nine V.A.M, Roeleveld, Nel, Franke, Barbara

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  5. 5
    Genetics of Hypospadias: Are Single-Nucleotide Polymorphisms in SRD5A2, ESR1, ESR2, and ATF3 Really Associated with the Malformation?

    Genetics of Hypospadias: Are Single-Nucleotide Polymorphisms in SRD5A2, ESR1, ESR2, and ATF3 Really Associated with the Malformation? by van der Zanden, Loes F. M., van Rooij, Iris A. L. M., Feitz, Wout F. J., Vermeulen, Sita H. H. M., Kiemeney, Lambertus A. L. M., Knoers, Nine V. A. M., Roeleveld, Nel, Franke, Barbara

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  6. 6
    An association study of 45 folate-related genes in spina bifida: Involvement of cubilin (CUBN) and tRNA aspartic acid methyltransferase 1 (TRDMT1)

    An association study of 45 folate-related genes in spina bifida: Involvement of cubilin (CUBN) and tRNA aspartic acid methyltransferase 1 (TRDMT1) by Franke, Barbara, Vermeulen, Sita H.H.M., Steegers-Theunissen, Regine P.M., Coenen, Marieke J., Schijvenaars, Mascha M.V.A.P., Scheffer, Hans, den Heijer, Martin, Blom, Henk J.

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  7. 7
    The methionine synthase reductase 66A>G polymorphism is a maternal risk factor for spina bifida

    The methionine synthase reductase 66A>G polymorphism is a maternal risk factor for spina bifida by VAN DER LINDEN, Ivon J. M, DEN HEIJER, Martin, AFMAN, Lydia A, GELLEKINK, Henkjan, VERMEULEN, Sita H. H. M, KLUIJTMANS, Leo A. J, BLOM, Henk J

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  8. 8
    Correlation of rheumatoid arthritis severity with the genetic functional variants and circulating levels of macrophage migration inhibitory factor

    Correlation of rheumatoid arthritis severity with the genetic functional variants and circulating levels of macrophage migration inhibitory factor by Radstake, Timothy R. D. J., Sweep, Fred C. G. J., Welsing, Paco, Franke, Barbara, Vermeulen, Sita H. H. M., Geurts‐Moespot, Anneke, Calandra, Thierry, Donn, Rachelle, van Riel, Piet L. C. M.

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