Menin interacts directly with the homeobox-containing protein Pem. by Lemmens, I, Forsberg, L, Pannett, A, Meyen, E, Piehl, F, Turner, J, Van de Ven, W, Thakker, R, Larsson, C, Kas, K

GATA3 haplo-insufficiency causes human HDR syndrome. by Van Esch, H, Groenen, P, Nesbit, M, Schuffenhauer, S, Lichtner, P, Vanderlinden, G, Harding, B, Beetz, R, Bilous, R, Holdaway, I, Shaw, N, Fryns, J, Van de Ven, W, Thakker, R, Devriendt, K

The search for the MEN1 gene. The European Consortium on MEN-1. by Lemmes, I, Van de Ven, W, Kas, K, Zhang, C, Giraud, S, Wautot, V, Buisson, N, Pugeat, M, Peix, J, Caldener, A, Parente, F, Quincey, D, Courseaux, A, Carle, G, Gaudray, P, De Wit, M, Lips, C, Hoppener, J, Khodaei, S, Grant, A, Weber, G, Teh, B, Farnebo, F, Kytola, S, Grimmond, S

Construction of a 1.2-Mb sequence-ready contig of chromosome 11q13 encompassing the multiple endocrine neoplasia type 1 (MEN1) gene by Lemmens, I, Merregaert, J, Van De Ven, W, Koen, K, Zhang, C, Giraud, S, Wautot, V, Buisson, N, De Witte, K, Salandre, J, Lenoir, G, Calender, A, Parente, F, Quincey, D, Courseaux, A, Carle, G, Gaudray, P, De Wit, M, Lips, C, Höppener, J, Khodaei, S, Grant, A, Weber, G, Kytölä, S, Teh, B

A putative human zinc-finger gene (ZFPL1) on 11q13, highly conserved in the mouse and expressed in exocrine pancreas. The European Consortium on MEN 1. by Höppener, J, De Wit, M, Simarro-Doorten, A, Roijers, J, van Herrewaarden, H, Lips, C, Parente, F, Quincey, D, Gaudray, P, Khodaei, S, Weber, G, Teh, B, Farnebo, F, Larsson, C, Zhang, C, Calender, A, Pannett, A, Forbes, SA, Bassett, J, Thakker, R, Lemmens, I, Van de Ven, W, Kas, K

Construction of a 1.2-Mb sequence-ready contig of chromosome 11q13 encompassing the multiple endocrine neoplasia type 1 (MEN1) gene. The European Consortium on MEN1. by Lemmens, I, Merregaert, J, Van de Ven, W, Kas, K, Zhang, C, Giraud, S, Wautot, V, Buisson, N, De Witte, K, Salandre, J, Lenoir, G, Calender, A, Parente, F, Quincey, D, Courseaux, A, Carle, G, Gaudray, P, De Wit, M, Lips, C, Höppener, J, Khodaei, S, Grant, A, Weber, G, Kytölä, S, Thakker, R

Identification of the multiple endocrine neoplasia type 1 (MEN1) gene. The European Consortium on MEN1. by Lemmens, I, Van de Ven, W, Kas, K, Zhang, C, Giraud, S, Wautot, V, Buisson, N, De Witte, K, Salandre, J, Lenoir, G, Pugeat, M, Calender, A, Parente, F, Quincey, D, Gaudray, P, De Wit, M, Lips, C, Höppener, J, Khodaei, S, Grant, A, Weber, G, Kytölä, S, Teh, B, Farnebo, F, Thakker, R