HER2 amplification status in breast cancer: a comparison between immunohistochemical staining and fluorescence in situ hybridisation using manual and automated quantitative image a... von Ellis, C M, Dyson, M J, Stephenson, T J, Maltby, E L

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An epidemiological study of Wolf-Hirschhorn syndrome: life expectancy and cause of mortality von Shannon, N L, Maltby, E L, Rigby, A S, Quarrell, O W J

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A case of deletion 14(q22.1-->q22.3) associated with anophthalmia and pituitary abnormalities von Elliott, J, Maltby, E L, Reynolds, B

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Elevated p53 expression in benign meningiomas protects against recurrence and may be indicative of senescence von Hakin-Smith, V., Battersby, R. D., Maltby, E. L., Timperley, W. R., Royds, J. A.

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Campomelic dysplasia associated with a de novo 2q;17q reciprocal translocation von Young, I D, Zuccollo, J M, Maltby, E L, Broderick, N J

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Xp21 muscular dystrophy due to X chromosome inversion von BAXTER, P. S, MALTBY, E. L, QUARRELL, O

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Detecting deletions in the critical region for lissencephaly on 17p13.3 using fluorescent in situ hybridisation and a PCR assay identifying a dinucleotide repeat polymorphism von Pilz, D T, Dalton, A, Long, A, Jaspan, T, Maltby, E L, Quarrell, O W

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Folate sensitive site at 10q23 and its expression as a deletion von Maltby, E L, Higgins, S

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Familial pericentric inversion (13) detected by antenatal diagnosis von Maltby, E L

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Inherited multiple meningiomas: a clinical, pathological and cytogenetic study of an affected family von Battersby, R D, Ironside, J W, Maltby, E L

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Duplication involving band 4q32 with minimal clinical effect von Maltby, Edna L., Barnes, Islay C.S., Bennett, Christopher P.

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Cytogenetic studies in 50 meningiomas von Maltby, Edna L., Ironside, James W., Battersby, Robert D.E.

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Folate-sensitive fragile site FRA10A is due to an expansion of a CGG repeat in a novel gene, FRA10AC1, encoding a nuclear protein von Sarafidou, Theologia, Kahl, Christina, Martinez-Garay, Isabel, Mangelsdorf, Marie, Gesk, Stefan, Baker, Elizabeth, Kokkinaki, Maria, Talley, Polly, Maltby, Edna L., French, Lisa, Harder, Lana, Hinzmann, Bernd, Nobile, Carlo, Richkind, Kathy, Finnis, Merran, Deloukas, Panagiotis, Sutherland, Grant R., Kutsche, Kerstin, Moschonas, Nicholas K., Siebert, Reiner, Gécz, Jozef

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Baller Gerold syndrome and Fanconi anaemia von Quarrell, Oliver W.J., Maltby, Edna L., Harrison, Christine J.

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An experimental investigation of pattern development in lethal spotting and belted mouse embryos von Mayer, Thomas C., Maltby, Ellen L.

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Detecting deletions in the critical region for lisencephaly on 17p13.3 using fluorescent in situ hybridisation and a PCR assay identifying a dinucleotide repeat polymorphism von PILZ, D. T, DALTON, A, LONG, A, JASPAN, T, MALTBY, E. L, QUARRELL, O. W. J

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Baller Gerold syndrome and Fanconi anaemia von Quarrell, O W, Maltby, E L, Harrison, C J

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RUBBER OVERSOLE von LE ROY MALTBY

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An ALMA Survey of the SCUBA-2 Cosmology Legacy Survey UKIDSS/UDS Field: Number Counts of Submillimeter Galaxies von Stach, Stuart M., Smail, Ian, Swinbank, A. M., Simpson, J. M., Geach, J. E., An, Fang Xia, Almaini, Omar, Arumugam, Vinodiran, Blain, A. W., Chapman, S. C., Chen, Chian-Chou, Conselice, C. J., Cooke, E. A., Coppin, K. E. K., Dunlop, J. S., Farrah, Duncan, Gullberg, B., Hartley, W., Ivison, R. J., Maltby, D. T., Micha owski, M. J., Scott, Douglas, Simpson, Chris, Thomson, A. P., Wardlow, J. L., Werf, P. van der

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An ALMA survey of the SCUBA-2 CLS UDS field: physical properties of 707 sub-millimetre galaxies von Dudzevičiūtė, U, Smail, Ian, Swinbank, A M, Stach, S M, Almaini, O, da Cunha, E, An, Fang Xia, Arumugam, V, Birkin, J, Blain, A W, Chapman, S C, Chen, C-C, Conselice, C J, Coppin, K E K, Dunlop, J S, Farrah, D, Geach, J E, Gullberg, B, Hartley, W G, Hodge, J A, Ivison, R J, Maltby, D T, Scott, D, Simpson, C J, Simpson, J M, Thomson, A P, Walter, F, Wardlow, J L, Weiss, A, van der Werf, P

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