A DGGE system for comprehensive mutation screening of BRCA1 and BRCA2: application in a Dutch cancer clinic setting by Hout, Annemarie H. van der, Ouweland, Ans M.W. van den, Luijt, Rob B. van der, Gille, Hans J.P., Bodmer, Daniëlle, Brüggenwirth, Hennie, Mulder, Inge M., Vlies, Pieter van der, Elfferich, Peter, Huisman, Maarten T., Berge, Annelies M. ten, Kromosoeto, Joan, Jansen, Rumo P.M., Zon, Patrick H.A. van, Vriesman, Thyrsa, Arts, Neeltje, Lange, Majella Boutmy-de, Oosterwijk, Jan C., Meijers-Heijboer, Hanne, Ausems, Margreet G.E.M., Hoogerbrugge, Nicoline, Verhoef, Senno, Halley, Dicky J.J., Vos, Yvonne J., Hogervorst, Frans, Ligtenberg, Marjolijn, Hofstra, Robert M.W.

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Discordant NIPT result in a viable trisomy‐21 pregnancy due to prolonged contribution to cfDNA by a demised trisomy‐14 cotwin by Hochstenbach, Ron, Elferink, Martin G., Zon, Patrick H. A., Lichtenbelt, Klaske D., Harssel, Jeske, Schuring‐Blom, Heleen, Page‐Christiaens, Godelieve C.M.L.

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Discordant NIPT result in a viable trisomy‐21 pregnancy due to prolonged contribution to cf DNA by a demised trisomy‐14 cotwin by Hochstenbach, Ron, Elferink, Martin G., van Zon, Patrick H. A., Lichtenbelt, Klaske D., van Harssel, Jeske, Schuring‐Blom, Heleen, Page‐Christiaens, Godelieve C.M.L.

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DNA analysis of AHI1 , NPHP1 and CYCLIN D1 in Joubert syndrome patients from the Netherlands by Kroes, Hester Y, van Zon, Patrick H.A, van de Putte, Dietje Fransen, Nelen, Marcel R, Nievelstein, Rutger-Jan, Wittebol-Post, Dienke, van Nieuwenhuizen, Onno, Mancini, Grazia M.S, van der Knaap, Marjo S, Kwee, Mei Lan, Maas, Saskia M, Cobben, Jan Maarten, De Nef, Jacques E.E, Lindhout, Dick, Sinke, Richard J

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De novo recurrent germline mutation of the BRCA2 gene in a patient with early onset breast cancer by VAN DER LUIJT, Rob B, VAN ZON, Patrick H. A, JANSEN, Rumö P. M, VAN DER SIJS-BOS, Carla J. M, WÄRLÄM-RODENHUIS, Carla C, AUSEMS, Margreet G. E. M

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DNA analysis of AHI1, NPHP1 and CYCLIN Dl in Joubert syndrome patients from the Netherlands by KROES, Hester Y, VAN ZON, Patrick H. A, MAAS, Saskia M, COBBEN, Jan Maarten, DE NEF, Jacques E. E, LINDHOUT, Dick, SINKE, Richard J, VAN DE PUTTE, Dietje Fransen, NELEN, Marcel R, NIEVELSTEIN, Rutger-Jan, WITTEBOL-POST, Dienke, VAN NIEUWENHUIZEN, Onno, MANCINI, Grazia M. S, VAN DER KNAAP, Marjo S, KWEE, Mei Lan

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De novo recurrent germline mutation of theBRCA2 gene in a patient with early onset breast cancer by van der Luijt, Rob B, van Zon, Patrick H A, Jansen, Rumó P M, van der Sijs-Bos, Carla J M, Wárlám-Rodenhuis, Carla C, Ausems, Margreet G E M

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Discordant NIPT result in a viable trisomy-21 pregnancy due to prolonged contribution to cfDNA by a demised trisomy-14 cotwin by Hochstenbach, Ron, Elferink, Martin G, van Zon, Patrick H A, Lichtenbelt, Klaske D, van Harssel, Jeske, Schuring-Blom, Heleen, Page-Christiaens, Godelieve C M L

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Symptom profiles and their risk factors in patients with post-COVID-19 condition: a Dutch longitudinal cohort study by van Zon, Sander K R, Ballering, Aranka V, Brouwer, Sandra, Rosmalen, Judith G M

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Motor performance and functional ability in preschool- and early school-aged children with Juvenile Idiopathic Arthritis: a cross-sectional study by van der Net, Janjaap, van der Torre, Patrick, Engelbert, Raoul Hh, Engelen, Vivian, van Zon, Femke, Takken, Tim, Helders, Paul Jm

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