Authors:
BENCH AJ
ALDRED MA
HUMPHRAY SJ
CHAMPION KM
GILBERT JGR
ASIMAKOPOULOS FA
DELOUKAS P
GWILLIAM R
BENTLEY DR
GREEN AR
Citation: Aj. Bench et al., A DETAILED PHYSICAL AND TRANSCRIPTIONAL MAP OF THE REGION OF CHROMOSOME-20 THAT IS DELETED IN MYELOPROLIFERATIVE DISORDERS AND REFINEMENT OF THE COMMON DELETED REGION, Genomics, 49(3), 1998, pp. 351-362
Authors:
BENCH AJ
ALDRED MA
HOLLOWAY TL
CHAMPION KM
GILBERT JGR
HUMPHRAY SJ
GWILLIAM R
DELOUKAS P
BENTLEY DR
NACHEVA EP
GREEN AR
Citation: Aj. Bench et al., TRANSCRIPT MAPPING OF THE REGION OF CHROMOSOME 20Q THAT IS DELETED INMYELOPROLIFERATIVE DISORDERS, British Journal of Haematology, 102(1), 1998, pp. 156-156
Citation: Ma. Aldred et al., DETECTION OF KNOWN MUTATIONS - TOWARDS PARALLEL-PROCESSING IN THE DIAGNOSTIC LABORATORY, American journal of human genetics, 61(4), 1997, pp. 1254-1254
Authors:
WRIGHT AF
DRY KI
EDGAR AJ
MANSON FDC
ALDRED MA
BROWN J
HO MF
LENNON A
HARDWICK LJ
MONACO AP
JAY M
BIRD AC
Citation: Af. Wright et al., ISOLATION OF A RETINAL-EXPRESSED GENE AND LINKAGE DISEQUILIBRIUM MAPPING IN THE RP3 TYPE X-LINKED RETINITIS-PIGMENTOSA REGION, Investigative ophthalmology & visual science, 37(3), 1996, pp. 4578-4578
Authors:
ASIMAKOPOULOS FA
GILBERT JGR
ALDRED MA
PEARSON TC
GREEN AR
Citation: Fa. Asimakopoulos et al., INTERSTITIAL DELETION CONSTITUTES THE MAJOR MECHANISM FOR LOSS OF HETEROZYGOSITY ON CHROMOSOME 20Q IN POLYCYTHEMIA-VERA, Blood, 88(7), 1996, pp. 2690-2698
Authors:
DRY KL
ALDRED MA
EDGAR AJ
BROWN J
MANSON FDC
HO MF
PROSSER J
HARDWICK LJ
LENNON AA
THOMSON K
VANKEUREN M
KURNIT DM
BIRD AC
JAY M
MONACO AP
WRIGHT AF
Citation: Kl. Dry et al., IDENTIFICATION OF A NOVEL GENE, ETX1, FROM XP21.1, A CANDIDATE GENE FOR X-LINKED RETINITIS-PIGMENTOSA (RP3), Human molecular genetics, 4(12), 1995, pp. 2347-2353
Authors:
ASIMAKOPOULOS FA
GILBERT JGR
ALDRED MA
MESSINEZY M
PEARSON TC
GREEN AR
Citation: Fa. Asimakopoulos et al., INTERSTITIAL DELETION CONSTITUTES THE MAJOR MECHANISM FOR LOSS OF HETEROZYGOSITY ON CHROMOSOME 20Q IN MYELOPROLIFERATIVE DISORDERS, Blood, 86(10), 1995, pp. 1320-1320
Authors:
ALDRED MA
HUMPHRAY SJ
GWILLIAM R
BENTLEY DR
GREEN AR
Citation: Ma. Aldred et al., A YAC CONTIG SPANNING THE REGION OF CHROMOSOME 20Q THAT IS DELETED INMYELOPROLIFERATIVE DISORDERS, American journal of human genetics, 57(4), 1995, pp. 1480-1480
Authors:
DRY KL
ALDRED MA
EDGAR AJ
MANSON FDC
BROWN J
PROSSER J
THOMSON KL
JAY M
BIRD AC
WRIGHT AF
Citation: Kl. Dry et al., ISOLATION OF A CANDIDATE GENE FOR X-LINKED RETINITIS-PIGMENTOSA (RP3), American journal of human genetics, 57(4), 1995, pp. 1501-1501
Authors:
ALDRED MA
TEAGUE PW
JAY M
BUNDEY S
REDMOND RM
JAY B
BIRD AC
BHATTACHARYA SS
WRIGHT AF
Citation: Ma. Aldred et al., RETINITIS-PIGMENTOSA FAMILIES SHOWING APPARENT X-LINKED INHERITANCE BUT UNLINKED TO THE RP2 OR RP3 LOCI, Journal of Medical Genetics, 31(11), 1994, pp. 848-852
Authors:
ALDRED MA
DRY KL
KNIGHTJONES EB
HARDWICK LJ
TEAGUE PW
LESTER DH
BROWN J
SPOWART G
CAROTHERS AD
RAEBURN JA
BIRD AC
FIELDER AR
WRIGHT AF
Citation: Ma. Aldred et al., GENETIC-ANALYSIS OF A KINDRED WITH X-LINKED MENTAL HANDICAP RETINITIS-PIGMENTOSA, American journal of human genetics, 55(5), 1994, pp. 916-922
Authors:
TEAGUE PW
ALDRED MA
JAY M
DEMPSTER M
HARRISON C
CAROTHERS AD
HARDWICK LJ
EVANS HJ
STRAIN L
BROCK DJH
BUNDEY S
JAY B
BIRD AC
BHATTACHARYA SS
WRIGHT AF
Citation: Pw. Teague et al., HETEROGENEITY ANALYSIS IN 40 X-LINKED RETINITIS-PIGMENTOSA FAMILIES, American journal of human genetics, 55(1), 1994, pp. 105-111
Authors:
DRY KL
VANDORP DB
ALDRED MA
BROWN J
HARDWICK LJ
WRIGHT AF
Citation: Kl. Dry et al., LINKAGE ANALYSIS IN A FAMILY WITH COMPLETE TYPE CONGENITAL STATIONARYNIGHT BLINDNESS WITH AND WITHOUT MYOPIA, Clinical genetics, 43(5), 1993, pp. 250-254
Authors:
HARDWICK LJ
BROWN J
DRY KL
LESTER DH
ALDRED MA
JAY M
BIRD AC
WRIGHT AF
Citation: Lj. Hardwick et al., ISOLATION OF MICROSATELLITE AND EXPRESSED SEQUENCES FROM A YEAST ARTIFICIAL CHROMOSOME FROM THE RP3 REGION USING BIOTIN-STREPTAVIDIN SELECTION, American journal of human genetics, 53(3), 1993, pp. 1300-1300