Use of restriction endonucleases to detect and isolate genes from mammalian cellsBICKMORE, W. A; BIRD, A. P.Methods in enzymology. 1992, Vol 216, pp 224-244, issn 0076-6879Article

Putting the genome on the mapBRIDGER, J. M; BICKMORE, W. A.Trends in genetics (Regular ed.). 1998, Vol 14, Num 10, pp 403-409, issn 0168-9525Article

The distribution of CpG islands in mammalian chromosomesCRAIG, J. M; BICKMORE, W. A.Nature genetics. 1994, Vol 7, Num 3, pp 376-382, issn 1061-4036Article

Imprinting mutations in the Beckwith-Wiedemann syndrome suggested by an altered imprinting pattern in the IGF2-H19 domainREIK, W; BROWN, K. W; SCHNEID, H et al.Human molecular genetics (Print). 1995, Vol 4, Num 12, pp 2379-2385, issn 0964-6906Article

Evolution of homologous sequences on the human X and Y chromosomes, outside of the meiotic pairing segmentBICKMORE, W. A; COOKE, H. J.Nucleic acids research. 1987, Vol 15, Num 15, pp 6261-6271, issn 0305-1048Article

Close linkage of the human cytochrome P450IIA and P450IIB gene subfamilies: implications for the assignment of substrate specificityMILES, J. S; BICKMORE, W; BROOK, J. D et al.Nucleic acids research. 1989, Vol 17, Num 8, pp 2907-2917, issn 0305-1048Article

Hitch-hiking from HRAS1 to the WAGR locus with GMGT markersBICKMORE, W; CHRISTIE, S; VAN HEYNINGEN, V et al.Nucleic acids research. 1988, Vol 16, Num 1, pp 51-60, issn 0305-1048Article

DNA binding capacity of the WT1 protein is abolished by Denys-Drash syndrome WT1 point mutationsLITTLE, M; HOLMES, G; BICKMORE, W et al.Human molecular genetics (Print). 1995, Vol 4, Num 3, pp 351-358, issn 0964-6906Article

The candidate Wilm's tumour gene in involoved in genitourinary developmentPRITCHARD-JONES, K; FLEMING, S; VAN HEYNINGER, V et al.Nature (London). 1990, Vol 346, Num 6280, pp 194-196, issn 0028-0836Article

Imprinting mutation in the Beckwith-Wiedemann syndrome leads to biallelic IGF2 expression through an H19-independent pathwayBROWN, K. W; VILLAR, A. J; BICKMORE, W et al.Human molecular genetics (Print). 1996, Vol 5, Num 12, pp 2027-2032, issn 0964-6906Article

Aniridia-associated cytogenetic rearrangements suggest that a position effect may cause the mutant phenotypeFANTES, J; REDEKER, B; DANES, S et al.Human molecular genetics (Print). 1995, Vol 4, Num 3, pp 415-422, issn 0964-6906Article

Dinucleotide repeat polymorphism at the D11S995 locusBROWNE, D. L; VAN HEYNINGEN, V; BICKMORE, W et al.Human molecular genetics (Print). 1993, Vol 2, Num 8, issn 0964-6906, p. 1332Article

HRAS1-selected chromosome transfer generates markers that colocalize aniridia- and gentiourinary dysplasia-associated translocation breakpoints and the Wilms tumor gene within band 11p13PORTEOUS, D. J; BICKMORE, W; VAN HEYMINGEN, V et al.Proceedings of the National Academy of Sciences of the United States of America. 1987, Vol 84, Num 15, pp 5355-5359, issn 0027-8424Article

Colocalization of the human CD59 gene to 11p13 with the MIC11 cell surface antigenBICKMORE, W. A; LONGBOTTOM, D; OGHENE, K et al.Genomics (San Diego, Calif.). 1993, Vol 17, Num 1, pp 129-135, issn 0888-7543Article

Long-range structure of H-ras l-selected transgenomesBICKMORE, W. A; MAULE, J. C; VAN HEYNINGEN, V et al.Somatic cell and molecular genetics. 1989, Vol 15, Num 3, pp 229-235, issn 0740-7750, 7 p.Article

Organization of the region encompassing the human serum amyloid A (SAA) gene family on chromosome 11q15.1SELLAR, G. C; OGHENE, K; BOYLE, S et al.Genomics (San Diego, Calif.). 1994, Vol 23, Num 2, pp 492-495, issn 0888-7543Article

The expression of the Wilms' tumour gene, WT1, in the developing mammalian embryoARMSTRONG, J. F; PRITCHARD-JONES, K; BICKMORE, W. A et al.Mechanisms of development. 1993, Vol 40, Num 1-2, pp 85-97, issn 0925-4773Article

Interspecific backross mice show sex-specific differences in allelic inheritanceSIRACUSA, L. D; ALVORD, W. G; BICKMORE, W. A et al.Genetics. 1991, Vol 128, Num 4, pp 813-821, issn 0016-6731Article

Modulation of DNA binding specificity by alternative splicing of the wilms tumor wt1 gene transcriptBICKMORE, W. A; OGHENE, K; LITTLE, M. H et al.Science (Washington, D.C.). 1992, Vol 257, Num 5067, pp 235-237, issn 0036-8075Article

Submicroscopic deletions at the WAGR locus, revealed by nonradioactive in situ hybridizationFANTES, J. A; BICKMORE, W. A; FLETCHER, J. M et al.American journal of human genetics. 1992, Vol 51, Num 6, pp 1286-1294, issn 0002-9297Article

The chromosomal distribution of CpG islands in the mouse : Evidence for genome scrambling in the rodent lineageCROSS, S. H; LEE, M; CLARK, V. H et al.Genomics (San Diego, Calif.). 1997, Vol 40, Num 3, pp 454-461, issn 0888-7543Article

The human serum amyloid A protein (SAA) superfamily gene cluster : mapping to chromosome 11p15.1 by physical and genetic linkage analysisSELLAR, G. C; JORDAN, S. A; BICKMORE, W. A et al.Genomics (San Diego, Calif.). 1994, Vol 19, Num 2, pp 221-227, issn 0888-7543Article

The reticulocalbin gene maps to the WAGR region in human and to the small eye Harwell deletion in mouseKENT, J; LEE, M; SCHEDL, A et al.Genomics (San Diego, Calif.). 1997, Vol 42, Num 2, pp 260-267, issn 0888-7543Article

Unusual chromosome structure of fission yeast DNA in mouse cellsMCMANUS, J; PERRY, P; SUMNER, A. T et al.Journal of Cell Science. 1994, Vol 107, pp 469-486, issn 0021-9533, 3Article

A Y chromosome gene family with RNA-binding protein homology : candidates for the azoospermia factor AZF controlling human spermatogenesisKUN MA; INGLIS, J. D; WOLFE, J et al.Cell (Cambridge). 1993, Vol 75, Num 7, pp 1287-1295, issn 0092-8674Article