Risultati della ricerca - Janssens, Katrien

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

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

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

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

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

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

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Mutations in the SPTLC2 Subunit of Serine Palmitoyltransferase Cause Hereditary Sensory and Autonomic Neuropathy Type I di 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

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