A large family with MSH3-related polyposis von Aelvoet, Arthur S., Hoekman, Daniël R., Redeker, Bert J. W., Weegenaar, Jitske, Dekker, Evelien, van Noesel, Carel J. M., Duijkers, Floor A. M.

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Activating germline R776H mutation in the epidermal growth factor receptor associated with lung cancer with squamous differentiation von van Noesel, Jan, van der Ven, Ward H, van Os, Theo A M, Kunst, Peter W A, Weegenaar, Jitske, Reinten, Roy J A, Kancha, Rama K, Duyster, Justus, van Noesel, Carel J M

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Dystrophin nonsense mutation induces different levels of exon 29 skipping and leads to variable phenotypes within one BMD family von Ginjaar, Ieke B, Kneppers, Alexander LJ, v d Meulen, Jan-Douwe M, Anderson, Louise VB, Bremmer-Bout, Mattie, van Deutekom, Judith CT, Weegenaar, Jitske, den Dunnen, Johan T, Bakker, Egbert

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Effects of Processing Delay, Formalin Fixation, and Immunohistochemistry on RNA Recovery From Formalin-fixed Paraffin-embedded Tissue Sections von van Maldegem, Febe, de Wit, Mireille, Morsink, Folkert, Musler, Alex, Weegenaar, Jitske, van Noesel, Carel J. M

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Dystrophin nonsense mutation induces different levels of exon 29 skipping and leads to variable phenotypes within one BMD family von Ginjaar, I B, Kneppers, A L, v d Meulen, J D, Anderson, L V, Bremmer-Bout, M, van Deutekom, J C, Weegenaar, J, den Dunnen, J T, Bakker, E

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Cultures of ovarian surface epithelium from women with and without a hereditary predisposition to develop female adnexal carcinoma von Piek, Jurgen M.J, Dorsman, Josephine C, Shvarts, Avi, Ansink, Anca C, Massuger, Leon F.A.G, Scholten, Piet, van Diest, Paul J, Dijkstra, Jan C, Weegenaar, Jitske, Kenemans, Peter, Verheijen, René H.M

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A novel 7·9 kb deletion causing α+‐thalassaemia in two independent families of Indian origin von Harteveld, Cornelis L., Van Delft, Peter, Wijermans, Pierre W., Kappers‐Klunne, Mies C., Weegenaar, Jitske, Losekoot, Monique, Giordano, Piero C.

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A novel 7.9 kb deletion causing α+-thalassaemia in two independent families of Indian origin von HARTEVELD, Cornelis L, VAN DELFT, Peter, WIJERMANS, Pierre W, KAPPERS-KLUNNE, Mies C, WEEGENAAR, Jitske, LOSEKOOT, Monique, GIORDANO, Piero C

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BRCA1 and p53 protein expression in cultured ovarian surface epithelial cells derived from women with and without a BRCA1 germline mutation von Piek, Jurgen M J, Dorsman, Josephine C, Massuger, Leon F, Ansink, Anca C, Weegenaar, Jitske, Shvarts, Avi, Kenemans, Peter, Verheijen, René H M

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Dystrophin nonsense mutation induces different levels of exon29 skipping and leads to variable phenotypes within one BMD family von Ginjaar, Ieke B, Kneppers, Alexander LJ, v d Meulen, Jan-Douwe M, Anderson, Louise VB, Bremmer-Bout, Mattie, van Deutekom, Judith CT, Weegenaar, Jitske, den Dunnen, Johan T, Bakker, Egbert

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