Treffer 1 - 7 von 7 für Suche 'Maiburg, Merel C', Suchdauer: 0,43s Treffer weiter einschränken
  1. 1
    Genetic Heterogeneity and Clinical Variability in Musculocontractural Ehlers-Danlos Syndrome Caused by Impaired Dermatan Sulfate Biosynthesis

    Genetic Heterogeneity and Clinical Variability in Musculocontractural Ehlers-Danlos Syndrome Caused by Impaired Dermatan Sulfate Biosynthesis von Syx, Delfien, Van Damme, Tim, Symoens, Sofie, Maiburg, Merel C., van de Laar, Ingrid, Morton, Jenny, Suri, Mohnish, Del Campo, Miguel, Hausser, Ingrid, Hermanns-Lê, Trinh, De Paepe, Anne, Malfait, Fransiska

    Veröffentlicht in Human mutation

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  2. 2
    Lethal neonatal bone marrow failure syndrome with multiple congenital abnormalities, including limb defects, due to a constitutional deletion of 3' MECOM

    Lethal neonatal bone marrow failure syndrome with multiple congenital abnormalities, including limb defects, due to a constitutional deletion of 3' MECOM von van der Veken, Lars T, Maiburg, Merel C, Groenendaal, Floris, van Gijn, Mariëlle E, Bloem, Andries C, Erpelinck, Claudia, Gröschel, Stefan, Sanders, Mathijs A, Delwel, Ruud, Bierings, Marc B, Buijs, Arjan

    Veröffentlicht in Haematologica (Roma)

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  3. 3
    Attitudes of Klinefelter men and their relatives towards TESE-ICSI

    Attitudes of Klinefelter men and their relatives towards TESE-ICSI von Maiburg, Merel C., Hoppenbrouwers, Alissia C., van Stel, Henk F., Giltay, Jacques C.


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  4. 4
    Lethal neonatal bone marrow failure syndrome with multiple congenital abnormalities, including limb defects, due to a constitutional deletion of 3’ MECOM

    Lethal neonatal bone marrow failure syndrome with multiple congenital abnormalities, including limb defects, due to a constitutional deletion of 3’ MECOM von van der Veken, Lars T, Maiburg, Merel C, Groenendaal, Floris, van Gijn, Mariëlle E, Bloem, Andries C, Erpelinck, Claudia, Gröschel, Stefan, Sanders, Mathijs A, Delwel, Ruud, Bierings, Marc B, Buijs, Arjan


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  5. 5
    Pancreatic cancer-associated gene polymorphisms in a nation-wide cohort of p16-Leiden germline mutation carriers; A case-control study Medical Genetics

    Pancreatic cancer-associated gene polymorphisms in a nation-wide cohort of p16-Leiden germline mutation carriers; A case-control study Medical Genetics von Potjer, Thomas P, Van Der Stoep, Nienke, Houwing-Duistermaat, Jeanine J, Konings, Ingrid C A W, Aalfs, Cora M, Van Den Akker, Peter C, Ausems, Margreet G, Dommering, Charlotte J, Van Der Kolk, Lizet E, Maiburg, Merel C, Spruijt, Liesbeth, Wagner, Anja, Vasen, Hans F A, Hes, Frederik J


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  6. 6
    Pancreatic cancer-associated gene polymorphisms in a nation-wide cohort of p16-Leiden germline mutation carriers; a case-control study

    Pancreatic cancer-associated gene polymorphisms in a nation-wide cohort of p16-Leiden germline mutation carriers; a case-control study von Potjer, Thomas P, van der Stoep, Nienke, Houwing-Duistermaat, Jeanine J, Konings, Ingrid C A W, Aalfs, Cora M, van den Akker, Peter C, Ausems, Margreet G, Dommering, Charlotte J, van der Kolk, Lizet E, Maiburg, Merel C, Spruijt, Liesbeth, Wagner, Anja, Vasen, Hans F A, Hes, Frederik J

    Veröffentlicht in BMC research notes

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  7. 7
    Novel Bone Marrow Failure Syndrome Due to a Deletion of the EVI1/Mecom Gene

    Novel Bone Marrow Failure Syndrome Due to a Deletion of the EVI1/Mecom Gene von van der Veken, Lars T., Bierings, Marc, Maiburg, Merel, Groenendaal, Floris, Bloem, Andries C, Knoers, Nine V., Buijs, Arjan

    Veröffentlicht in Blood

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