Torthaí cuardaigh - Janssens, Katrien

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  1. 1
    Direct detection of guidance receptor activity during border cell migration

    Direct detection of guidance receptor activity during border cell migration de réir Janssens, Katrien, Sung, Hsin-Ho, Rørth, Pernille

    Foilsithe / Cruthaithe 2010
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  2. 2
    Prenatal homozygosity mapping detects a novel mutation in CHST3 in a fetus with skeletal dysplasia and joint dislocations

    Prenatal homozygosity mapping detects a novel mutation in CHST3 in a fetus with skeletal dysplasia and joint dislocations de réir Muys, Joke, Blaumeiser, Bettina, Jacquemyn, Yves, Janssens, Katrien

    Foilsithe / Cruthaithe 2017
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  3. 3
    Terminal deletion of chromosome 13 in a fetus with normal NIPT: The added value of invasive prenatal diagnosis in the NIPT era

    Terminal deletion of chromosome 13 in a fetus with normal NIPT: The added value of invasive prenatal diagnosis in the NIPT era de réir Vervecken, Evy, Blaumeiser, Bettina, Vanderheyden, Tina, Hauspy, Jan, Janssens, Katrien

    Foilsithe / Cruthaithe 2020
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  4. 4
    Characterization of EVL-I as a protein kinase D substrate

    Characterization of EVL-I as a protein kinase D substrate de réir Janssens, Katrien, De Kimpe, Line, Balsamo, Michele, Vandoninck, Sandy, Vandenheede, Jackie R., Gertler, Frank, Van Lint, Johan

    Foilsithe / Cruthaithe 2008
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  5. 5
    Genetic Testing Contributes to Diagnosis in Cerebral Palsy: Aicardi-Goutières Syndrome as an Example

    Genetic Testing Contributes to Diagnosis in Cerebral Palsy: Aicardi-Goutières Syndrome as an Example de réir Beysen, Diane, De Cordt, Chania, Dielman, Charlotte, Ogunjimi, Benson, Dandelooy, Julie, Reyniers, Edwin, Janssens, Katrien, Meuwissen, Marije M.E.

    Foilsithe / Cruthaithe 2021
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  6. 6
    Cell-Free DNA From Metastatic Pancreatic Neuroendocrine Tumor Patients Contains Tumor-Specific Mutations and Copy Number Variations

    Cell-Free DNA From Metastatic Pancreatic Neuroendocrine Tumor Patients Contains Tumor-Specific Mutations and Copy Number Variations de réir Boons, Gitta, Vandamme, Timon, Peeters, Marc, Beyens, Matthias, Driessen, Ann, Janssens, Katrien, Zwaenepoel, Karen, Roeyen, Geert, Van Camp, Guy, Op de Beeck, Ken

    Foilsithe / Cruthaithe 2018
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  7. 7
    Mutations in the SPTLC2 Subunit of Serine Palmitoyltransferase Cause Hereditary Sensory and Autonomic Neuropathy Type I

    Mutations in the SPTLC2 Subunit of Serine Palmitoyltransferase Cause Hereditary Sensory and Autonomic Neuropathy Type I de réir Rotthier, Annelies, Auer-Grumbach, Michaela, Janssens, Katrien, Baets, Jonathan, Penno, Anke, Almeida-Souza, Leonardo, Van Hoof, Kim, Jacobs, An, De Vriendt, Els, Schlotter-Weigel, Beate, Löscher, Wolfgang, Vondráček, Petr, Seeman, Pavel, De Jonghe, Peter, Van Dijck, Patrick, Jordanova, Albena, Hornemann, Thorsten, Timmerman, Vincent

    Foilsithe / Cruthaithe 2010
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