Localisation of human alpha globin to 16p13.3----pter.

od Buckle, V J, Higgs, D R, Wilkie, A O, Super, M, Weatherall, D J
Wydane 1988

Structure of the human DNA repair gene HAP1 and its localisation to chromosome 14q 11.2-12.

od Robson, C N, Hochhauser, D, Craig, R, Rack, K, Buckle, V J, Hickson, I D
Wydane 1992

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

od Gibbons, R J, Suthers, G K, Wilkie, A O, Buckle, V J, Higgs, D R
Wydane 1992

Localisation of Y chromosome sequences in normal and 'XX' males.

od Buckle, V J, Boyd, Y, Fraser, N, Goodfellow, P N, Goodfellow, P J, Wolfe, J, Craig, I W
Wydane 1987

Telomere directed fragmentation of mammalian chromosomes.

od Barnett, M A, Buckle, V J, Evans, E P, Porter, A C, Rout, D, Smith, A G, Brown, W R
Wydane 1993

Loss of both CSF1R (FMS) alleles in patients with myelodysplasia and a chromosome 5 deletion.

od Boultwood, J, Rack, K, Kelly, S, Madden, J, Sakaguchi, A Y, Wang, L M, Oscier, D G, Buckle, V J, Wainscoat, J S
Wydane 1991

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

od Morrison, K E, Daniels, R J, Suthers, G K, Flynn, G A, Francis, M J, Buckle, V J, Davies, K E
Wydane 1992

Identification of the FRAXE fragile site in two families ascertained for X linked mental retardation.

od Flynn, G A, Hirst, M C, Knight, S J, Macpherson, J N, Barber, J C, Flannery, A V, Davies, K E, Buckle, V J
Wydane 1993

Clinical features and molecular analysis of the alpha thalassemia/mental retardation syndromes. II. Cases without detectable abnormality of the alpha globin complex.

od Wilkie, A O, Zeitlin, H C, Lindenbaum, R H, Buckle, V J, Fischel-Ghodsian, N, Chui, D H, Gardner-Medwin, D, MacGillivray, M H, Weatherall, D J, Higgs, D R
Wydane 1990

Localization of a putative transcriptional regulator (ATRX) at pericentromeric heterochromatin and the short arms of acrocentric chromosomes

od McDowell, T. L., Gibbons, R. J., Sutherland, H., O’Rourke, D. M., Bickmore, W. A., Pombo, A., Turley, H., Gatter, K., Picketts, D. J., Buckle, V. J., Chapman, L., Rhodes, D., Higgs, D. R.
Wydane 1999

Characterization of three de novo derivative chromosomes 16 by “Reverse chromosome painting” and molecular analysis

od Rack, K. A., Harris, P. C., MacCarthy, A. B., Boone, R., Raynham, H., McKinley, M., Fitchett, M., Towe, C. M., Rudd, P., Armour, J. A. L., Lindenbaum, R. H., Buckle, V. J.
Wydane 1993

Clinical features and molecular analysis of the α thalassemia/mental retardation syndromes. 1. Cases due to deletions involving chromosome band 16p13.3

od Wilkie, A. O. M., Buckle, V. J., Harris, P. C., Lamb, J., Barton, N. J., Reeders, S. T., Lindenbaum, R. H., Nicholls, R. D., Barrow, M., Bethlenfalvay, N. C., Hutz, M. H., Tolmie, J. L., Weatherall, D. J., Higgs, D. R.
Wydane 1990