Torthaí cuardaigh - Suthers, G K

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

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

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

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

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

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

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

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

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

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

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

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

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Prenatal prediction of spinal muscular atrophy. de réir Daniels, R J, Suthers, G K, Morrison, K E, Thomas, N H, Francis, M J, Mathew, C G, Loughlin, S, Heiberg, A, Wood, D, Dubowitz, V

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Physical mapping of new DNA probes near the fragile X mutation (FRAXA) by using a panel of cell lines de réir Suthers, G. K., Hyland, V. J., Callen, D. F., Oberle, I., Rocchi, M., Thomas, N. S., Morris, C. P., Schwartz, C. E., Schmidt, M., Ropers, H. H., Baker, E., Oostra, B. A., Dahl, N., Wilson, P. J., Hopwood, J. J., Sutherland, G. R.

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Genetic mapping of new DNA probes at Xq27 defines a strategy for DNA studies in the fragile X syndrome de réir Suthers, G. K., Mulley, J. C., Voelckel, M. A., Dahl, N., Väisänen, M. L., Steinbach, P., Glass, I. A., Schwartz, C. E., van Oost, B. A., Thibodeau, S. N., Haites, N. E., Oostra, B. A., Giné, R., Carballo, M., Morris, C. P., Hopwood, J. J., Sutherland, G. R.

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