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Results: 1-5 |
Results: 5

Authors: Moog, U De Die-Smulders, CEM Schrander-Stumpel, CTRM Engelen, JJM Hamers, AJH Frints, S Fryns, JP
Citation: U. Moog et al., Holoprosencephaly: The Maastricht experience, GEN COUNSEL, 12(3), 2001, pp. 287-298

Authors: Jun, L Frints, S Duhamel, H Herold, A Abad-Rodrigues, J Dotti, C Izaurralde, E Marynen, P Froyen, G
Citation: L. Jun et al., NXF5, a novel member of the nuclear RNA export factor family, is lost in amale patient with a syndromic form of mental retardation, CURR BIOL, 11(18), 2001, pp. 1381-1391

Authors: Zemni, R Bienvenu, T Vinet, MC Sefiani, A Carrie, A Billuart, P McDonell, N Couvert, P Francis, F Chafey, P Fauchereau, F Friocourt, G des Portes, V Cardona, A Frints, S Meindl, A Brandau, O Ronce, N Moraine, C van Bokhoven, H Ropers, HH Sudbrak, R Kahn, A Fryns, JP Beldjord, R Chelly, J
Citation: R. Zemni et al., A new gene involved in X-linked mental retardation identified by analysis of an X;2 balanced translocation, NAT GENET, 24(2), 2000, pp. 167-170

Authors: Veugelers, M De Cat, B Muyldermans, SY Reekmans, G Delande, N Frints, S Legius, E Fryns, JP Schrander-Stumpel, C Weidle, B Magdalena, N David, G
Citation: M. Veugelers et al., Mutational analysis of the GPC3/GPC4 glypican gene cluster on Xq26 in patients with Simpson-Golabi-Behmel syndrome: identification of loss-of-function mutations in the GPC3 gene, HUM MOL GEN, 9(9), 2000, pp. 1321-1328

Authors: Carrie, A Jun, L Bienvenu, T Vinet, MC McDonell, N Couvert, P Zemni, R Cardona, A Van Buggenhout, G Frints, S Hamel, B Moraine, C Ropers, HH Strom, T Howell, GR Whittaker, A Ross, MT Kahn, A Fryns, JP Beldjord, C Marynen, P Chelly, J
Citation: A. Carrie et al., A new member of the IL-1 receptor family highly expressed in hippocampus and involved in X-linked mental retardation, NAT GENET, 23(1), 1999, pp. 25-31
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