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Poustka, A, Dietrich, A, Langenstein, G, Toniolo, D, Warren, ST and Lehrach, H: Physical map of human Xq27-qter: Localizing the region of the fragile X mutation. Proceedings of the National Academy of Sciences, USA 88:8302-8306 (1991).
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Pieretti, M, Fu, Y-H, Warren, ST, Zhang, F, Oostra, BA, Caskey, CT and Nelson, DL: Absence of expression of the FMR-1 gene in fragile X syndrome. Cell 66:817-822 (1991).
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Kremer, EJ, Pritchard, M, Lynch, M, Yu, S, Holman, K, Baker, E, Warren, ST, Schlessinger, D, Sutherland, GR and Richards, RI: Mapping of DNA instability at the fragile X to a trinucleotide repeat sequence p(CCG)n. Science 252:1711-1714 (1991).
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Dietrich, A, Kioschis, P, Monaco, AP, Gross, B, Korn, B, Williams, SV, Sheer, D, Heitz, D, Oberle, I, Toniolo, D, Warren, ST, Lehrach, H and Poustka, A: Molecular cloning and analysis of the fragile X region in man. Nucleic Acids Research 19:2567-2572 (1991). |
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Yu, S, Kremer, E, Pritchard, M, Lynch, M, Nancarrow, J, Baker, E, Holman, K, Mulley, JC, Warren, ST, Schlessinger, D, Sutherland, GR and Richards, RI: The fragile X genotype is characterized by an unstable region of DNA. Science 252:1179-1181 (1991).
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Verkerk, AJMH, Pieretti, M, Sutcliffe, JS, Fu, Y-H, Kuhl, DPA, Pizzuti, A, Reiner, O, Richards, S, Victoria, MF, Zhang, F, Eussen, BE, van Ommen, GLB, Blonden, LAJ, Riggins, GJ, Chastain, JL, Kunst, CB, Gakljaard, H, Caskey, CT, Nelson, DL, Oostra, BA and Warren, ST: Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome. Cell 65:905-914 (1991).
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Hirst, MC, Roche, A, Flint, TJ, MacKinnin, R, Bassett, JHD, Nakahori, Y, Watson, JEV, Bell, MV, Patterson, MN, Boyd, Y, Thomas, N, Knight, SJL, Warren, ST, Hors-Cayla, M, Schmidt, M, Sutherland, GR and Davies, KE: Linear order of new and established DNA markers around the fragile site at Xq27.3. Genomics 10:243-249 (1991).
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Consalez, G., Thomas, NST, Stayton, C, Knight, SJL, Johnson, M, Hopkins LC, Harper, PS, Elsas, LJ and Warren, ST: Assignment of Emery-Dreifuss muscular dystrophy to the distal region of Xq28: The results of a collaborative study. American Journal of Human Genetics 48:468-480 (1991).
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Rousseau, F, Vincent, A, Toniolo, D, Heitz, D, Warren, ST, Suthers, GK, Goodfellow, P, Mandel, JL and Oberle, I: Four chromosomal breakpoints and four new probes mark out a 10 cM region encompassing the FRAXA locus. American Journal of Human Genetics 48:108-116 (1991).
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