Search Results - Whatley, S.D.

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  1. 1
    Clinical experience of scoring criteria for Familial Hypercholesterolaemia (FH) genetic testing in Wales

    Clinical experience of scoring criteria for Familial Hypercholesterolaemia (FH) genetic testing in Wales by Haralambos, K, Whatley, S.D, Edwards, R, Gingell, R, Townsend, D, Ashfield-Watt, P, Lansberg, P, Datta, D.B.N, McDowell, I.F.W

    Published in Atherosclerosis
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  2. 2
    Five year experience of scoring criteria for familial hypercholesterolaemia (FH) genetic testing in wales: Should the criteria be refined to include age?

    Five year experience of scoring criteria for familial hypercholesterolaemia (FH) genetic testing in wales: Should the criteria be refined to include age? by Haralambos, K, Ashfield-Watt, P, Edwards, R, Gingell, R, Townsend, D, Whatley, S.D, Datta, D.B.N, McDowell, I.F.W

    Published in Atherosclerosis
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  3. 3
    GENETIC VARIANTS OF UNCERTAIN SIGNIFICANCE (VUS) IN FAMILIAL HYPERCHOLESTEROLAEMIA (FH) IN WALES: YEAR 2 UPDATE

    GENETIC VARIANTS OF UNCERTAIN SIGNIFICANCE (VUS) IN FAMILIAL HYPERCHOLESTEROLAEMIA (FH) IN WALES: YEAR 2 UPDATE by Haralambos, K, Whatley, S.D, Edwards, R, Gingell, R, Townsend, D, Holmans, P, Clarke, A, Datta, D.B.N, Butler, R, Palmer-Smith, S, Wood, M, McDowell, I.F.W

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  4. 4
    Genetic variants of uncertain significance (VUS) in familial hypercholesterolaemia (FH): Can family based association studies help determine pathogenicity?

    Genetic variants of uncertain significance (VUS) in familial hypercholesterolaemia (FH): Can family based association studies help determine pathogenicity? by Haralambos, K, Whatley, S.D, Edwards, R, Gingell, R, Townsend, D, Holmans, P, Clarke, A, Datta, B.N, McDowell, I.F.W

    Published in Atherosclerosis
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  5. 5
    Familial hypercholesterolaemia (FH) in Wales is genetically heterogeneous

    Familial hypercholesterolaemia (FH) in Wales is genetically heterogeneous by Haralambos, K, Whatley, S.D, Datta, B.N, Townsend, D, Gingell, R, Edwards, R, Lansberg, P, Graham, C, Palacios, L, Dean, P, McDowell, I.F.W

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  6. 6
    Sporadic case of fatal encephalopathy with neonatal onset associated with a T158M missense mutation in MECP2

    Sporadic case of fatal encephalopathy with neonatal onset associated with a T158M missense mutation in MECP2 by Lynch, S A, Whatley, S D, Ramesh, V, Sinha, S, Ravine, D

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  7. 7
    De-novo mutation and sporadic presentation of acute intermittent porphyria

    De-novo mutation and sporadic presentation of acute intermittent porphyria by Whatley, S.D., Roberts, A.G., Elder, G.H.

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  8. 8
    The effect of aspartame as part of a multidisciplinary weight-control program on short- and long-term control of body weight

    The effect of aspartame as part of a multidisciplinary weight-control program on short- and long-term control of body weight by Blackburn, GL, Kanders, BS, Lavin, PT, Keller, SD, Whatley, J

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