Rezultati pretrage - Knegt, Alida C

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Detaljiziraj rezultate
  1. 1
    Absence epilepsy and the CHD2 gene: an adolescent male with moderate intellectual disability, short-lasting psychoses, and an interstitial deletion in 15q26.1–q26.2

    Absence epilepsy and the CHD2 gene: an adolescent male with moderate intellectual disability, short-lasting psychoses, and an interstitial deletion in 15q26.1–q26.2 od Verhoeven, Willem MA, Egger, Jos IM, Knegt, Alida C, Zuydam, José, Kleefstra, Tjitske

    Izdano 2016
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  2. 2
    Prenatal diagnosis of a trisomy 7/trisomy 13 mosaicism

    Prenatal diagnosis of a trisomy 7/trisomy 13 mosaicism od Huijsdens-van Amsterdam, Karin, Barge-Schaapveld, Daniela QCM, Mathijssen, Inge B, Alders, Mariëlle, Pajkrt, Eva, Knegt, Alida C

    Izdano 2012
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  3. 3
    Prenatal sonographic features can accurately determine parental origin in triploid pregnancies

    Prenatal sonographic features can accurately determine parental origin in triploid pregnancies od Lugthart, Malou A., Horenblas, Judith, Kleinrouweler, Emily C., Engels, Melanie, Knegt, Alida C., Huijsdens, Karin, van Leeuwen, Elisabeth, Pajkrt, Eva

    Izdano 2020
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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 od 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

    Izdano 2005
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  5. 5
    Genetic basis of hyperlysinemia

    Genetic basis of hyperlysinemia od Houten, Sander M, te Brinke, Heleen, Denis, Simone, Ruiter, Jos PN, Knegt, Alida C, de Klerk, Johannis BC, Augoustides-Savvopoulou, Persephone, Häberle, Johannes, Baumgartner, Matthias R, Coşkun, Turgay, Zschocke, Johannes, Sass, Jörn Oliver, Poll-The, Bwee Tien, Wanders, Ronald JA, Duran, Marinus

    Izdano 2013
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  6. 6
    The prevalence of genetic diagnoses in fetuses with severe congenital heart defects

    The prevalence of genetic diagnoses in fetuses with severe congenital heart defects od van Nisselrooij, Amber E. L., Lugthart, Malou A., Clur, Sally-Ann, Linskens, Ingeborg H., Pajkrt, Eva, Rammeloo, Lukas A., Rozendaal, Lieke, Blom, Nico A., van Lith, Jan M. M., Knegt, Alida C., Hoffer, Mariëtte J. V., Aten, Emmelien, Santen, Gijs W. E., Haak, Monique C.

    Izdano 2020
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