Search Results - Suthers, G

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  1. 1
    Estimation of an approximate confidence interval for FRAXA location by using linkage data from many pedigrees.

    Estimation of an approximate confidence interval for FRAXA location by using linkage data from many pedigrees. by Suthers, G

    Published 1991
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  2. 2
    Skewed sex ratios in familial holoprosencephaly and in people with isolated single maxillary central incisor

    Skewed sex ratios in familial holoprosencephaly and in people with isolated single maxillary central incisor by Suthers, G., Smith, S., Springbett, S.

    Published 1999
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  3. 3
    Genetic counseling in rare syndromes: a resampling method for determining an approximate confidence interval for gene location with linkage data from a single pedigree.

    Genetic counseling in rare syndromes: a resampling method for determining an approximate confidence interval for gene location with linkage data from a single pedigree. by Suthers, G K, Wilson, S R

    Published 1990
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  4. 4
    Phenotypic heterogeneity and the single gene.

    Phenotypic heterogeneity and the single gene. by Suthers, G K, Davies, K E

    Published 1992
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  5. 5
    A BclI RFLP for DXS296 (VK21) near the fragile X

    A BclI RFLP for DXS296 (VK21) near the fragile X by Yu, S., Suthers, G.K., Mulley, J.C.

    Published 1990
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  6. 6
    Instability versus predictability: the molecular diagnosis of myotonic dystrophy.

    Instability versus predictability: the molecular diagnosis of myotonic dystrophy. by Suthers, G K, Huson, S M, Davies, K E

    Published 1992
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  7. 7
    Arteriovenous malformations in Cowden syndrome

    Arteriovenous malformations in Cowden syndrome by Turnbull, M, Humeniuk, V, Stein, B, Suthers, G

    Published 2005
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  8. 8
    Letting the family know: balancing ethics and effectiveness when notifying relatives about genetic testing for a familial disorder

    Letting the family know: balancing ethics and effectiveness when notifying relatives about genetic testing for a familial disorder by Suthers, G K, Armstrong, J, McCormack, J, Trott, D

    Published 2006
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  9. 9
    TaqI RFLP identified by probe 1A1 [DXS374] at Xq28.

    TaqI RFLP identified by probe 1A1 [DXS374] at Xq28. by Suthers, G K, Davies, K E, Baker, E, Sutherland, G R

    Published 1989
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  10. 10
    Becker muscular dystrophy (BMD) and Klinefelter's syndrome: a possible cause of variable expression of BMD within a pedigree.

    Becker muscular dystrophy (BMD) and Klinefelter's syndrome: a possible cause of variable expression of BMD within a pedigree. by Suthers, G K, Manson, J I, Stern, L M, Haan, E A, Mulley, J C

    Published 1989
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  11. 11
    X-linked alpha-thalassemia/mental retardation (ATR-X) syndrome: localization to Xq12-q21.31 by X inactivation and linkage analysis.

    X-linked alpha-thalassemia/mental retardation (ATR-X) syndrome: localization to Xq12-q21.31 by X inactivation and linkage analysis. by Gibbons, R J, Suthers, G K, Wilkie, A O, Buckle, V J, Higgs, D R

    Published 1992
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  12. 12
    Sorting nexin 3 (SNX3) is disrupted in a patient with a translocation t(6;13)(q21;q12) and microcephaly, microphthalmia, ectrodactyly, prognathism (MMEP) phenotype

    Sorting nexin 3 (SNX3) is disrupted in a patient with a translocation t(6;13)(q21;q12) and microcephaly, microphthalmia, ectrodactyly, prognathism (MMEP) phenotype by Vervoort, V, Viljoen, D, Smart, R, Suthers, G, DuPont, B, Abbott, A, Schwartz, C

    Published 2002
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  13. 13
    Attitudes to genetic testing for breast cancer susceptibility in women at increased risk of developing hereditary breast cancer

    Attitudes to genetic testing for breast cancer susceptibility in women at increased risk of developing hereditary breast cancer by MEISER, B., BUTOW, P., BARRATT, A., SUTHERS, G., SMITH, M., COLLEY, A., THOMPSON, E., TUCKER, K.

    Published 2000
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  14. 14
    TaqI RFLP identified by probe VK17A (DXS294) at Xq26.

    TaqI RFLP identified by probe VK17A (DXS294) at Xq26. by Suthers, G K, Hyland, V J, Baker, E, Fernandez, K E, Callen, D F, Sutherland, G R

    Published 1988
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  15. 15
    Most germ-line mutations in the nevoid basal cell carcinoma syndrome lead to a premature termination of the PATCHED protein, and no genotype-phenotype correlations are evident.

    Most germ-line mutations in the nevoid basal cell carcinoma syndrome lead to a premature termination of the PATCHED protein, and no genotype-phenotype correlations are evident. by Wicking, C, Shanley, S, Smyth, I, Gillies, S, Negus, K, Graham, S, Suthers, G, Haites, N, Edwards, M, Wainwright, B, Chenevix-Trench, G

    Published 1997
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  16. 16
    High-resolution genetic map around the spinal muscular atrophy (SMA) locus on chromosome 5.

    High-resolution genetic map around the spinal muscular atrophy (SMA) locus on chromosome 5. by Morrison, K E, Daniels, R J, Suthers, G K, Flynn, G A, Francis, M J, Buckle, V J, Davies, K E

    Published 1992
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  17. 17
    Tailoring communication in consultations with women from high risk breast cancer families

    Tailoring communication in consultations with women from high risk breast cancer families by Lobb, E A, Butow, P N, Meiser, B, Barratt, A, Gaff, C, Young, M A, Kirk, J, Suthers, G K, Tucker, K

    Published 2002
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  18. 18
    Communication and information-giving in high-risk breast cancer consultations: influence on patient outcomes

    Communication and information-giving in high-risk breast cancer consultations: influence on patient outcomes by Lobb, E A, Butow, P N, Barratt, A, Meiser, B, Gaff, C, Young, M A, Haan, E, Suthers, G, Gattas, M, Tucker, K

    Published 2004
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  19. 19
    Four chromosomal breakpoints and four new probes mark out a 10-cM region encompassing the fragile-X locus (FRAXA)

    Four chromosomal breakpoints and four new probes mark out a 10-cM region encompassing the fragile-X locus (FRAXA) by Rousseau, F., Vincent, A., Rivella, S., Heitz, D., Triboli, C., Maestrini, E., Warren, S. T., Suthers, G. K., Goodfellow, P., Mandel, J. L., Toniolo, D., Oberle, I.

    Published 1991
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  20. 20
    The challenges of finding the gene responsible for a rare, autosomal dominant gastric cancer susceptibility syndrome

    The challenges of finding the gene responsible for a rare, autosomal dominant gastric cancer susceptibility syndrome by Li, JJ, Healey, S, Phillips, K, Makunin, I, Wayte, N, Schrader, I, Worthley, D, Lindor, N, Huntsman, D, Goldgar, D, Suthers, G, Chenevix-Trench, G

    Published 2012
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