Authors:
WALLACE DF
PARTRIDGE J
ROBERTSON A
SIMPSON VMA
WORWOOD M
BOMFORD AB
VOLZ A
ZIEGLER A
DOOLEY JS
WALKER AP
Citation: Df. Wallace et al., A 6P22 REFERENCE MAP OF LEUKOCYTE DNA - EXCLUSION OF REARRANGEMENT IN4 CASES OF ATYPICAL HEMOCHROMATOSIS, European journal of human genetics, 6(5), 1998, pp. 523-526
Citation: Gh. Elder et M. Worwood, MUTATIONS IN THE HEMOCHROMATOSIS GENE, PORPHYRIA-CUTANEA-TARDA, AND IRON OVERLOAD, Hepatology, 27(1), 1998, pp. 289-291
Authors:
WORWOOD M
BOWEN DJ
BURNETT AK
JACKSON HA
LAWLESS S
RAHACHOWDHURY R
SHEARMAN JD
WALLACE DF
DOOLEY JS
PARTRIDGE J
WALKER AP
BOMFORD A
ROSENBERG WMC
MERRYWEATHERCLARKE AT
ROBSON KJH
POINTON JJ
Citation: M. Worwood et al., H63D IS AN HEMOCHROMATOSIS ASSOCIATED ALLELE - REPLY, Gut, 43(3), 1998, pp. 441-442
Authors:
MERRYWEATHERCLARKE AT
WORWOOD M
PARKINSON L
MATTOCK C
POINTON JJ
SHEARMAN JD
ROBSON KJH
Citation: At. Merryweatherclarke et al., THE EFFECT OF HFE MUTATIONS ON SERUM FERRITIN AND TRANSFERRIN SATURATION IN THE JERSEY POPULATION, British Journal of Haematology, 101(2), 1998, pp. 369-373
Authors:
ROBERTS AG
WHATLEY SD
NICKLIN S
WORWOOD M
POINTON JJ
STONE C
ELDER GH
Citation: Ag. Roberts et al., THE FREQUENCY OF HEMOCHROMATOSIS-ASSOCIATED ALLELES IS INCREASED IN BRITISH PATIENTS WITH SPORADIC PORPHYRIA-CUTANEA-TARDA, Hepatology, 25(1), 1997, pp. 159-161
Authors:
ROBERTS AG
WHATLEY SD
MORGAN RR
WORWOOD M
ELDER GH
Citation: Ag. Roberts et al., INCREASED FREQUENCY OF THE HEMOCHROMATOSIS CYS282TYR MUTATION IN SPORADIC PORPHYRIA-CUTANEA-TARDA, Lancet, 349(9048), 1997, pp. 321-323
Authors:
ROBSON KJH
WORWOOD M
SHEARMAN JD
WALLACE DF
DOOLEY JS
MERRYWEATHERCLARKE AT
POINTON JJ
ROSENBERG WMC
BOWEN DJ
BURNETT AK
JACKSON HA
LAWLESS S
RAHACHOWDHURY R
PARTRIDGE J
WILLIAMS R
BOMFORD A
WALKER A
Citation: Kjh. Robson et al., A SIMPLE GENETIC TEST IDENTIFIES 90-PERCENT OF UK PATIENTS WITH HEMOCHROMATOSIS, Gut, 41(6), 1997, pp. 841-844
Authors:
THORPE SJ
WALKER D
AROSIO P
HEATH A
COOK JD
WORWOOD M
Citation: Sj. Thorpe et al., INTERNATIONAL COLLABORATIVE STUDY TO EVALUATE A RECOMBINANT L-FERRITIN PREPARATION AS AN INTERNATIONAL STANDARD, Clinical chemistry, 43(9), 1997, pp. 1582-1587
Citation: Ha. Jackson et al., RAPID GENETIC SCREENING FOR HEMOCHROMATOSIS USING HETERODUPLEX TECHNOLOGY, British Journal of Haematology, 98(4), 1997, pp. 856-859
Authors:
WORWOOD M
CHOWDHURY RR
ROBSON KJH
POINTON J
SHEARMAN JD
DARKE C
Citation: M. Worwood et al., THE HLA A1-B8 HAPLOTYPE EXTENDS 6 MB BEYOND HLA-A - ASSOCIATIONS BETWEEN HLA-A, HLA-B, HLA-F AND 15 MICROSATELLITE MARKERS, Tissue antigens, 50(5), 1997, pp. 521-526
Citation: R. Rahachowdhury et al., A NEW HIGHLY POLYMORPHIC MARKER IN THE 5'-UNTRANSLATED REGION OF HLA-F SHOWS STRONG ALLELIC ASSOCIATION WITH HEMOCHROMATOSIS, Human genetics, 97(2), 1996, pp. 228-231
Authors:
DARKE C
FUSSELL H
STREET J
THOMAS M
GUTTRIDGE MG
WORWOOD M
Citation: C. Darke et al., SEROLOGICAL AND MOLECULAR-IDENTIFICATION OF AN HLA-B8 VARIANT, HLA-B8JON(B-ASTERISK-0802), Experimental and clinical immunogenetics, 13(3-4), 1996, pp. 139-153
Citation: M. Worwood et al., IRON-ABSORPTION FROM A NATURAL MINERAL-WATER (SPATONE IRON-PLUS), Clinical and laboratory haematology, 18(1), 1996, pp. 23-27
Authors:
RAHACHOWDHURY R
MOORE CA
BRADLEY D
HENLEY R
WORWOOD M
Citation: R. Rahachowdhury et al., BLOOD FERRITIN CONCENTRATIONS IN NEWBORN-INFANTS AND THE SUDDEN-INFANT-DEATH-SYNDROME, Journal of Clinical Pathology, 49(2), 1996, pp. 168-170
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SHEARMAN J
POINTON JJ
MERRYWEATHERCLARKE A
STONE C
ROSENBERG W
ROBSON K
WEATHERALL DJ
BOMFORD A
WILLIAMS R
WALKER A
DOOLEY J
RAHACHOWDHURY R
WORWOOD M
Citation: J. Shearman et al., LOCALIZATION OF THE HEMOCHROMATOSIS GENE LOCUS, Gastroenterology, 110(4), 1996, pp. 1320-1320
Authors:
WORWOOD M
DORAK MT
NICKLIN S
STONE C
POINTON J
DARKE C
Citation: M. Worwood et al., THE FREQUENCY OF THE HEMOCHROMATOSIS-ASSOCIATED GENOTYPE D6S265-1-D6S105-8 IN BLOOD-DONORS, British Journal of Haematology, 93(4), 1996, pp. 838-840
Authors:
WHITE AD
JONES BM
WORWOOD M
WEBB DKH
DAVIES KR
CLARK V
BURNETT AK
Citation: Ad. White et al., MONITORING DISEASE STATUS IN PEDIATRIC ACUTE LYMPHOBLASTIC-LEUKEMIA (ALL) USING CONVENTIONAL CYTOGENETIC TECHNIQUES, FLUORESCENCE IN-SITU HYBRIDIZATION (FISH) AND PCR DETECTION OF IGH GENE REARRANGEMENTS (CDR3), Blood, 88(10), 1996, pp. 285-285