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Results: 1-18 |
Results: 18

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

Authors: COHEN RV ALDRED MA PAES WS FAUSTO AMF NUCCI JR YOSHIMURA EM OKUNO E GARCIA ME MARUTA LM TOLOSA EMC
Citation: Rv. Cohen et al., HOW SAFE IS ERCP TO THE ENDOSCOPIST, Surgical endoscopy, 11(6), 1997, pp. 615-617

Authors: ALDRED MA SPENCE L MITCHELL VE
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: BROWN J DRY KL EDGAR AJ PRYDE FE HARDWICK LJ ALDRED MA LESTER DH BOYLE S KAPLAN J DUFIER JL HO MF MONACO AM MUSARELLA MA WRIGHT AF
Citation: J. Brown et al., ANALYSIS OF 3 DELETION BREAKPOINTS IN XP21.1 AND THE FURTHER LOCALIZATION OF RP3, Genomics, 37(2), 1996, pp. 200-210

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 WRIGHT AF
Citation: Ma. Aldred et Af. Wright, HAPLOTYPE FREQUENCIES OF 3 POLYMORPHISMS AT THE TIMP LOCUS, Molecular and cellular probes, 8(4), 1994, pp. 333-334

Authors: ALDRED MA DRY KL SHARP DM VANDORP DB BROWN J HARDWICK LJ LESTER DH PRYDE FE TEAGUE PW JAY M BIRD AC JAY B WRIGHT AF
Citation: Ma. Aldred et al., LINKAGE ANALYSIS IN X-LINKED CONGENITAL STATIONARY NIGHT BLINDNESS (VOL 14, PG 99, 1992), Genomics, 22(1), 1994, pp. 255-255

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
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