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Prenatal Diagnosis|November 1, 1985
A survey of diagnostic amniocenteses in Oxford from 1974-1981E Terzian, J Boreham, H S Cuckle, et al.Journal of Molecular Biology|July 25, 1997
Expression of the dystrophin-related protein 2 (Drp2) transcript in the mouseA K Dixon, T M Tait, E A Campbell, et al.Neuromuscular Disorders : NMD|January 1, 1992
Linkage of Emery-Dreifuss muscular dystrophy to the red/green cone pigment (RGCP) genes, proximal to factor VIIIC G Cole, S J Abbs, V Dubowitz, et al.Journal of Medical Genetics|March 1, 1989
Spontaneous and induced chromosome breakage in chorionic villus samples: a cytogenetic approach to first trimester prenatal diagnosis of ataxia telangiectasia syndromeJ Llerena, M Murer-Orlando, M McGuire, et al.Lancet (London, England)|February 6, 1988
Prenatal testing for Duchenne and Becker muscular dystrophyC G Cole, A Walker, A Coyne, et al.Journal of Medical Genetics|December 1, 1986
The screening of Duchenne muscular dystrophy patients for submicroscopic deletionsK Hart, C Cole, A Walker, et al.Annals of Human Genetics|May 1, 1976
Evidence for the assignment of the loci AK1, AK3 and ACONs to chromosome 9 in manS Povey, C A Slaughter, D E Wilson, et al.Human Molecular Genetics|February 1, 1993
The identification of a third fragile site, FRAXF, in Xq27--q28 distal to both FRAXA and FRAXEM C Hirst, A Barnicoat, G Flynn, et al.Genomics|October 1, 1992
A random STS strategy for construction of YAC contigs spanning defined chromosomal regionsC G Cole, I Dunham, A J Coffey, et al.British Journal of Obstetrics and Gynaecology|March 1, 1979
Clinical dilemmas arising from the antenatal diagnosis of neural tube defectsG M Stirrat, A C Turnbull, M J Bennett, et al.Pageof 423