Search Results - Murday, V.A.

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  1. 1
    An Ancestral Ashkenazi Haplotype at the HMPS/CRAC1 Locus on 15q13–q14 Is Associated with Hereditary Mixed Polyposis Syndrome

    An Ancestral Ashkenazi Haplotype at the HMPS/CRAC1 Locus on 15q13–q14 Is Associated with Hereditary Mixed Polyposis Syndrome by Jaeger, E.E.M., Woodford-Richens, K.L., Lockett, M., Rowan, A.J., Sawyer, E.J., Heinimann, K., Rozen, P., Murday, V.A., Whitelaw, S.C., Ginsberg, A., Atkin, W.S., Lynch, H.T., Southey, M.C., Debinski, H., Eng, C., Bodmer, W.F., Talbot, I.C., Hodgson, S.V., Thomas, H.J.W., Tomlinson, I.P.M.

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  2. 2
    A Gene for Lymphedema-Distichiasis Maps to 16q24.3

    A Gene for Lymphedema-Distichiasis Maps to 16q24.3 by Mangion, J., Rahman, N., Mansour, S., Brice, G., Rosbotham, J., Child, A.H., Murday, V.A., Mortimer, P.S., Barfoot, R., Sigurdsson, A., Edkins, S., Sarfarazi, M., Burnand, K., Evans, A.L., Nunan, T.O., Stratton, M.R., Jeffery, S.

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  3. 3
    Genetic Predisposition to Cancer: The Consequences of a Delayed Diagnosis of Gorlin Syndrome

    Genetic Predisposition to Cancer: The Consequences of a Delayed Diagnosis of Gorlin Syndrome by Mitchell, G., Farndon, P.A., Brayden, P., Murday, V.A., Eeles, R.A.

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  4. 4
    Linkage of recessive Robinow syndrome to a 4 cM interval on chromosome 9q22

    Linkage of recessive Robinow syndrome to a 4 cM interval on chromosome 9q22 by AFZAL, A. R, RAJAB, A, FENSKE, C, CROSBY, A, LAHIRI, N, TERNES-PEREIRA, E, MURDAY, V. A, HOULSTON, R, PATTON, M. A, JEFFERY, S

    Published in Human genetics
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  5. 5
    Incontinentia pigmenti in a surviving male is accompanied by hypohidrotic ectodermal dysplasia and recurrent infection

    Incontinentia pigmenti in a surviving male is accompanied by hypohidrotic ectodermal dysplasia and recurrent infection by Mansour, S., Woffendin, H., Mitton, S., Jeffery, I., Jakins, T., Kenwrick, S., Murday, V.A.

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  6. 6
    Linkage of recessive Robinow syndrome to a 4 cM interval on chromosome 9q22

    Linkage of recessive Robinow syndrome to a 4 cM interval on chromosome 9q22 by Afzal, A.R., Rajab, A., Fenske, C., Crosby, A., Lahiri, N., Ternes-Pereira, E., Murday, V.A., Houlston, R., Patton, M.A., Jeffery, S.

    Published in Human genetics
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  7. 7
    Linkage analysis of early-onset breast and ovarian cancer families, with markers on the long arm of chromosome 17

    Linkage analysis of early-onset breast and ovarian cancer families, with markers on the long arm of chromosome 17 by SPURR, N. K, KELSELL, D. P, BLACK, D. M, MURDAY, V. A, TURNER, G, CROCKFORD, G. P, SOLOMON, E, CARTWRIGHT, R. A, BISHOP, D. T

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  8. 8
    Incontinentia pigmenti in a surviving male is accompanied by hypohidrotic ectodermal dysplasia and recurrent infection

    Incontinentia pigmenti in a surviving male is accompanied by hypohidrotic ectodermal dysplasia and recurrent infection by Mansour, S., Woffendin, H., Mitton, S., Jeffery, I., Jakins, T., Kenwrick, S., Murday, V.A.

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