Authors:
POMFRET M
GOULD CP
BOURN D
MILLIGAN DW
WATERS JJ
Citation: M. Pomfret et al., IDENTIFICATION OF PML-RARA FUSION IN A CASE OF APL WITH A COMPLEX KARYOTYPE, Journal of Medical Genetics, 34, 1997, pp. 241-241
Authors:
WATERS J
BARLOW A
KEOHANE A
BOURN D
COLE T
TURNER B
Citation: J. Waters et al., A MOLECULAR CYTOGENETIC INVESTIGATION OF X-CHROMOSOME INACTIVATION INA 10-YEAR-OLD WITH A 46,X,DER(X) T(X-6)(P11.2-P21.1)MAT KARYOTYPE, Journal of Medical Genetics, 34, 1997, pp. 1203-1203
Authors:
WATERHOUSE RN
BUHARIWALLA H
BOURN D
RATTRAY EJ
GLOVER LA
Citation: Rn. Waterhouse et al., CCD DETECTION OF LUX-MARKED PSEUDOMONAS-SYRINGAE PV PHASEOLICOLA L-FORMS ASSOCIATED WITH CHINESE-CABBAGE AND THE RESULTING DISEASE PROTECTION AGAINST XANTHOMONAS-CAMPESTRIS, Letters in applied microbiology, 22(4), 1996, pp. 262-266
Authors:
EVANS DGR
BOURN D
WALLACE A
RAMSDEN RT
MITCHELL JD
STRACHAN T
Citation: Dgr. Evans et al., DIAGNOSTIC ISSUES IN A FAMILY WITH LATE-ONSET TYPE-2 NEUROFIBROMATOSIS, Journal of Medical Genetics, 32(6), 1995, pp. 470-474
Authors:
BOURN D
MASON S
TEKES S
CARTER SA
EVANS DGR
STRACHAN T
Citation: D. Bourn et al., MUTATION SCREENING AND GENOTYPE-PHENOTYPE CORRELATION IN NF2 PATIENTS, Journal of Medical Genetics, 32(2), 1995, pp. 138-138
Authors:
BOURN D
MASON S
TEKES S
TRUEMAN LA
CARTER SA
EVANS DGR
STRACHAN T
Citation: D. Bourn et al., MUTATION SCREENING AND FURTHER CHARACTERIZATION OF THE NF2 TUMOR-SUPPRESSOR GENE, American journal of human genetics, 57(4), 1995, pp. 316-316
Citation: D. Bourn et al., IDENTIFYING AND CHARACTERIZING PATHOLOGICAL MUTATIONS IN THE NF2 GENE, Journal of Medical Genetics, 31(2), 1994, pp. 168-168
Authors:
BOURN D
CARTER SA
EVANS DGR
GOODSHIP J
COAKHAM H
STRACHAN T
Citation: D. Bourn et al., A MUTATION IN THE NEUROFIBROMATOSIS TYPE-2 TUMOR-SUPPRESSOR GENE, GIVING RISE TO WIDELY DIFFERENT CLINICAL PHENOTYPES IN 2 UNRELATED INDIVIDUALS, American journal of human genetics, 55(1), 1994, pp. 69-73
Authors:
STRACHAN T
BOURN D
CARTER S
CARETTE M
WATSON C
HARRIS R
EVANS DGR
Citation: T. Strachan et al., IDENTIFYING AND CHARACTERIZING MUTATIONS IN THE MERLIN GENE IN PATIENTS WITH TYPE-2 NEUROFIBROMATOSIS, American journal of human genetics, 53(3), 1993, pp. 372-372