PAX6 mutations in aniridia von M.Hanson, Isabel, Seawright, Anne, Hardman, Karen, Hodgson, Shirley, Zaletayev, Dmitri, Fekete, Gyorgy, Heyningen, Veronica van

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Heterozygous Mutations of OTX2 Cause Severe Ocular Malformations von Ragge, Nicola K., Brown, Alison G., Poloschek, Charlotte M., Lorenz, Birgit, Henderson, R. Alex, Clarke, Michael P., Russell-Eggitt, Isabelle, Fielder, Alistair, Gerrelli, Dianne, Martinez-Barbera, Juan Pedro, Ruddle, Piers, Hurst, Jane, Collin, J. Richard O., Salt, Alison, Cooper, Simon T., Thompson, Pamela J., Sisodiya, Sanjay M., Williamson, Kathleen A., FitzPatrick, David R., Heyningen, Veronica van, Hanson, Isabel M.

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PAX6 and congenital eye malformations von HANSON, Isabel M

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Mammalian homologues of the Drosophila eye specification genes von Hanson, Isabel M

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Dose verification of dynamic MLC-tracked radiotherapy using small PRESAGE (R) 3D dosimeters and a motion phantom von Costa, F, Menten, MJ, Doran, S, Adamovics, J, Hanson, IM, Nill, S, Oelfke, U

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Polymicrogyria and absence of pineal gland due to PAX6 mutation von Mitchell, Tejal N., Free, Samantha L., Williamson, Kathleen A., Stevens, John M., Churchill, Amanda J., Hanson, Isabel M., Shorvon, Simon D., Moore, Anthony T., van Heyningen, Veronica, Sisodiya, Sanjay M.

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PAX6 haploinsufficiency causes cerebral malformation and olfactory dysfunction in humans von Sisodiya, Sanjay M, Free, Samantha L, Williamson, Kathleen A, Mitchell, Tejal N, Willis, Catherine, Stevens, John M, Kendall, Brian E, Shorvon, Simon D, Hanson, Isabel M, Moore, Anthony T, van Heyningen, Veronica

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Mutations at the PAX6 locus are found in heterogeneous anterior segment malformations including Peters' anomaly von Hanson, Isabel M, Fletcher, Judy M, Jordan, Tim, Brown, Alison, Taylor, David, Adams, Rebecca J, Punnett, Hope H, van Heyningen, Veronica

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A novel cysteine-rich sequence motif von Freemont, P S, Hanson, I M, Trowsdale, J

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Mouse Small eye results from mutations in a paired-like homeobox-containing gene von Hill, Robert E, Favor, Jack, Hogan, Brigid L. M, Ton, Carl C. T, Saunders, Grady F, Hanson, Isabel M, Prosser, Jane, Jordan, Tim, Hastie, Nicholas D, Heyningen, Veronica van

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Identification and Preliminary Characterization of a Protein Motif Related to the Zinc Finger von Lovering, Ruth, Hanson, Isabel M., Borden, Katherine L., Martin, Stephen, O'Reilly, Nicola J., Evan, Gerard I., Rahman, Dinah, Darryl J. C. Pappin, Trowsdale, John, Freemont, Paul S.

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Value and accuracy of cytology in addition to histology in the diagnosis of lung cancer at flexible bronchoscopy von JONES, A.M., HANSON, I.M., ARMSTRONG, G.R., O'DRISCOLL, B.R.

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Cognitive functioning in humans with mutations of the PAX6 gene von THOMPSON, P. J, MITCHELL, T. N, FREE, S. L, WILLIAMSON, K. A, HANSON, I. M, VAN HEYNINGEN, V, MOORE, A. T, SISODIYA, S. M

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PAX6 mutations: genotype-phenotype correlations von Tzoulaki, Ioanna, White, Ian M S, Hanson, Isabel M

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A study of eleven cutaneous malignant melanomas in adults with small-cell morphology: emphasis on diagnostic difficulties and unusual features von Hanson, I M, Banerjee, S S, Menasce, L P, Prescott, R J

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Evidence of nerve sheath differentiation and high grade morphology in sclerosing epithelioid fibrosarcoma von Hanson, I M, Pearson, J M, Eyden, B P, Slawik, S, Harris, M

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Prenatal diagnosis of aniridia von Churchill, Amanda J, Hanson, Isabel M, Markham, Alexander F

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Anal intraepithelial neoplasia in an inflammatory cloacogenic polyp von Hanson, I M, Armstrong, G R

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The human BDNF gene maps between FSHB and HVBS1 at the boundary of 11p13–p14 von Hanson, Isabel M., Seawright, Anne, van Heyningen, Veronica

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Colinearity of novel genes in the class II regions of the MHC in mouse and human von HANSON, I. M, TROWSDALE, J

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