Maternal segregation of the Dutch preeclampsia locus at 10q22 with a new member of the winged helix gene family
Oudejans, Cees B M, van Dijk, Marie, Mulders, Joyce, Poutsma, Ankie, Könst, Andrea A M, Lachmeijer, Augusta M A, Dekker, Gustaaf A, Blankenstein, Marinus A
Published in Nature genetics (01.05.2005)
Published in Nature genetics (01.05.2005)
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Mutations in each of the five subunits of translation initiation factor eIF2B can cause leukoencephalopathy with vanishing white matter
van der Knaap, Marjo S., Leegwater, Peter A. J., Könst, Andrea A.M., Visser, Allerdien, Naidu, Sakkubai, Oudejans, Cees B.M., Schutgens, Ruud B.H., Pronk, Jan C.
Published in Annals of neurology (01.02.2002)
Published in Annals of neurology (01.02.2002)
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Mutations of MLC1 ( KIAA0027), Encoding a Putative Membrane Protein, Cause Megalencephalic Leukoencephalopathy with Subcortical Cysts
Leegwater, Peter A.J., Yuan, Bao Qiang, van der Steen, Jeffrey, Mulders, Joyce, Könst, Andrea A.M., Boor, P. K. Ilja, Mejaski-Bosnjak, Vlatka, van der Maarel, Silvère M., Frants, Rune R., Oudejans, Cees B.M., Schutgens, Ruud B.H., Pronk, Jan C., van der Knaap, Marjo S.
Published in American journal of human genetics (01.04.2001)
Published in American journal of human genetics (01.04.2001)
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The parent-of-origin effect of 10q22 in pre-eclamptic females coincides with two regions clustered for genes with down-regulated expression in androgenetic placentas
Oudejans, Cees B.M., Mulders, Joyce, Lachmeijer, Augusta M.A., van Dijk, Marie, Könst, Andrea A.M., Westerman, Bart A., van Wijk, Inge J., Leegwater, Peter A.J., Kato, Hidenori D., Matsuda, Takao, Wake, Norio, Dekker, Gustaaf A., Pals, Gerard, ten Kate, Leo P., Blankenstein, Marinus A.
Published in Molecular human reproduction (01.08.2004)
Published in Molecular human reproduction (01.08.2004)
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identification of novel mutations in MLC1 responsible for megalencephalic leukoencephalopathy with subcortical cysts
LEEGWATER, P. A. J, BOOR, P. K. I, YUAN, B. Q, VAN DER STEEN, J, VISSER, A, KÖNST, A. A. M, OUDEJANS, C. B. M, SCHUTGENS, R. B. H, PRONK, J. C, VAN DER KNAAP, M. S
Published in Human genetics (01.03.2002)
Published in Human genetics (01.03.2002)
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Subunits of the translation initiation factor eLF2B are mutant in leukoencephalopathy with vanishing white matter
LEEGWATER, Peter A. J, VERMEULEN, Gerre, LEMMERS, Richard J. L. F, FRANTS, Rune R, OUDEJANS, Cees B. M, SCHUTGENS, Ruud B. H, PRONK, Jan C, VAN DER KNAAP, Marjo S, JULIER, Cecile, KÖNST, Andrea A. M, NAIDU, Sakkubai, MULDERS, Joyce, VISSER, Allerdien, KERSBERGEN, Paula, MOBACH, Dragosh, FONDS, Dafna, VAN BERKEL, Carola G. M
Published in Nature genetics (01.12.2001)
Published in Nature genetics (01.12.2001)
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The Gene for Leukoencephalopathy with Vanishing White Matter Is Located on Chromosome 3q27
Leegwater, Peter A.J., Könst, Andrea A.M., Kuyt, Bertus, Sandkuijl, Lodewijk A., Naidu, SakkuBai, Oudejans, Cees B.M., Schutgens, Ruud B.H., Pronk, Jan C., van der Knaap, Marjo S.
Published in American journal of human genetics (01.09.1999)
Published in American journal of human genetics (01.09.1999)
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Enrichment of fetal trophoblast cells from the maternal peripheral blood followed by detection of fetal deoxyribonucleic acid with a nested X/Y polymerase chain reaction
van Wijk, Inge J., van Vugt, John M.G., Mulders a, Monique A.M., Könst a, Andrea A.M., Weima, Sjerp M., Oudejans, Cees B.M.
Published in American journal of obstetrics and gynecology (01.03.1996)
Published in American journal of obstetrics and gynecology (01.03.1996)
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