检索结果 - 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. 由 Suthers, G K, Wilson, S R

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

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

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Instability versus predictability: the molecular diagnosis of myotonic dystrophy. 由 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 由 Suthers, G K, Armstrong, J, McCormack, J, Trott, D

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TaqI RFLP identified by probe 1A1 [DXS374] at Xq28. 由 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. 由 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. 由 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. 由 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. 由 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 由 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) 由 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. 由 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 由 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 由 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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