Dinucleotide repeat polymorphism at the D16S288 locus (1991)
Shen, Y., Holman, K., Thompson, A., Kozman, H., Callen, D.F., Sutherland, G.R., ...
Dinucleotide repeat polymorphism at the D16S288 locus (1991)
Shen, Y, Holman, K, Thompson, A, Kozman, H, Callen, DF, Sutherland, GR, ...
Dinucleotide repeat polymorphism at the D16S288 locus
Shen, Y., Holman, K., Thompson, A., Kozman, H., Callen, D.F., Sutherland, G.R., ...
Fragile X syndrome: diagnosis using highly polymorphic microsatellite markers.
Richards, R I, Shen, Y, Holman, K, Kozman, H, Hyland, V J, Mulley, J C, ...
We describe two highly polymorphic microsatellite AC repeat sequences, VK23AC and VK14AC, which are closely linked to the fragile X at Xq27.3. Both VK23AC (DXS297) and VK14AC (DXS292) are proximal to...
Dinucleotide repeat polymorphism at the D16S288 locus
Shen, Y., Holman, K., Thompson, A., Kozman, H., Callen, D.F., Sutherland, G.R., ...
Fragile X syndrome: diagnosis using highly polymorphic microsatellite markers.
Richards, R I, Shen, Y, Holman, K, Kozman, H, Hyland, V J, Mulley, J C, ...
We describe two highly polymorphic microsatellite AC repeat sequences, VK23AC and VK14AC, which are closely linked to the fragile X at Xq27.3. Both VK23AC (DXS297) and VK14AC (DXS292) are proximal to...
Autosomal dominant distal myopathy: linkage to chromosome 14.
Laing, N G, Laing, B A, Meredith, C, Wilton, S D, Robbins, P, Honeyman, K, ...
We have studied a family segregating a form of autosomal dominant distal myopathy (MIM 160500) and containing nine living affected individuals. The myopathy in this family is closest in clinical...
Richards, R I, Holman, K, Kozman, H, Kremer, E, Lynch, M, Pritchard, M, ...
We report the genetic localisation of the fragile site at Xq27.3 associated with fragile X syndrome. The position of the fragile site within the multipoint linkage map was determined using two...