PERITONEAL TUBERCULOSIS WITH URETERIC OBSTRUCTION, MIMICKING RETROPERITONEAL FIBROSISBENTLEY PG; HIGGS DR.1976; BRIT. J. UROL.; G.B.; DA. 1976; VOL. 48; NO 3; PP. 170; BIBL. 3 REF.Article

HAEMOGLOBIN CONSTANT SPRING HAS AN UNSTABLE ALPHA CHAIN MESSENGER RNAHUNT DM; HIGGS DR; WINICHAGOON P et al.1982; BR. J. HAEMATOL.; ISSN 0007-1048; GBR; DA. 1982; VOL. 51; NO 3; PP. 405-413; BIBL. 16 REF.Article

ALPHA -GLOBIN GENE DELETIONS ASSOCIATED WITH HB J TONGARIKIBOWDEN DK; PRESSLEY L; HIGGS DR et al.1982; BR. J. HAEMATOL.; ISSN 0007-1048; GBR; DA. 1982; VOL. 51; NO 2; PP. 243-249; BIBL. 7 REF.Article

MOLECULAR BASIS FOR MILD FORMS OF HOMOZYGONS BETA-THALASSAEMIAWEATHERALL DJ; PRESSLEY L; WOOD WG et al.1981; LANCET (BR. ED.); ISSN 0140-6736; GBR; DA. 1981; VOL. 1; NO 8219; PP. 527-529; BIBL. 9 REF.Article

A NOVEL ALPHA -GLOBIN GENE ARRANGEMENT IN MANHIGGS DR; OLD JM; PRESSLEY L et al.1980; NATURE; GBR; DA. 1980; VOL. 284; NO 5757; PP. 632-634; BIBL. 15 REF.Article

THE SIGNIFICANCE OF HAEMOGLOBIN H IN PATIENTS WITH MENTAL RETARDATION OR MYELOPROLIFERATIVE DISEASEWEATHERALL DJ; HIGGS DR; CLEGG JB et al.1982; BR. J. HAEMATOL.; ISSN 0007-1048; GBR; DA. 1982; VOL. 52; NO 3; PP. 351-355; BIBL. 12 REF.Article

HIGHLY VARIABLE REGIONS OF DNA FLANK THE HUMAN ALPHA GLOBIN GENESHIGGS DR; GOODBOURN SEY; WAINSCOAT JS et al.1981; NUCLEIC ACIDS RES.; ISSN 0305-1048; GBR; DA. 1981; VOL. 9; NO 17; PP. 4213-4224; BIBL. 15 REF.Article

A NEW TRIPLICATED ALPHA -GLOBIN GENE ARRANGEMENT IN MANTRENT RJ; HIGGS DR; CLEGG JB et al.1981; BR. J. HAEMATOL.; ISSN 0007-1048; GBR; DA. 1981; VOL. 49; NO 1; PP. 149-152; BIBL. 6 REF.Article

GGAMMA BETA ⁺ TYPE OF HEREDITARY PERSISTENCE OF FETAL HAEMOGLOBIN IN ASSOCIATION WITH HBCHIGGS DR; CLEGG JB; WOOD WG et al.1979; J. MED. GENET.; GBR; DA. 1979; VOL. 16; NO 4; PP. 288-295; BIBL. 2 P.Article

THE MOLECULAR BASIS FOR THE HAEMOGLOBIN BART'S HYDROPS FETALIS SYNDROME IN CYPRUSSOPHOCLEOUS T; HIGGS DR; ALDRIDGE B et al.1981; BR. J. HAEMATOL.; ISSN 0007-1048; GBR; DA. 1981; VOL. 47; NO 1; PP. 153-156; BIBL. 9 REF.Article

CHARACTERISATION OF A NEW ALPHA THALASSEMIA 1 DEFECT DUE TO A PARTIAL DELETION OF THE ALPHA GLOBIN GENE COMPLEXPRESSLEY L; HIGGS DR; ALDRIDGE B et al.1980; NUCLEIC ACIDS RES.; ISSN 0305-1048; GBR; DA. 1980; VOL. 8; NO 21; PP. 4889-4898; BIBL. 16 REF.Article

DETECTION OF ALPHA THALASSAEMIA IN NEGRO INFANTSHIGGS DR; PRESSLEY L; CLEGG JB et al.1980; BR. J. HAEMATOL.; ISSN 0007-1048; GBR; DA. 1980; VOL. 46; NO 1; PP. 39-46; BIBL. 19 REF.Article

MULTIPLE ARRANGEMENTS OF THE HUMAN EMBRYONIC DZETA GLOBIN GENESWINICHAGOON P; HIGGS DR; GOODBOURN SEY et al.1982; NUCLEIC ACIDS RES.; ISSN 0305-1048; GBR; DA. 1982; VOL. 10; NO 19; PP. 5853-5868; BIBL. 25 REF.Article

THALASSAEMIA INTERMEDIA IN CYPRUS: THE INTERACTION OF ALPHA AND BETA THALASSAEMIAWAINSCOAT JS; KANAVAKIS E; WOOD WG et al.1983; BRITISH JOURNAL OF HAEMATOLOGY; ISSN 0007-1048; GBR; DA. 1983; VOL. 53; NO 3; PP. 411-416; BIBL. 14 REF.Article

HEMOGLOBIN H DISEASE AND MENTAL RETARDATION: A NEW SYNDROME OR A REMARKABLE COINCIDENCE.WEATHERALL DJ; HIGGS DR; BUNCH C et al.1981; N. ENGL. J. MED.; ISSN 0028-4793; USA; DA. 1981; VOL. 305; NO 11; PP. 607-612; BIBL. 20 REF.Article

HAEMOGLOBIN BART'S HYDROPS SYNDROME IN GREECEKATTAMIS C; METAXOTOU MAVROMATI A; TSIARTIA E et al.1980; BRIT. MED. J.; GBR; DA. 1980; VOL. 281; NO 6235; PP. 268-270; BIBL. 14 REF.Article

GENETIC AND MOLECULAR DIVERSITY IN NONDELETION HB H DISEASEHIGGS DR; PRESSLEY L; ALDRIDGE B et al.1981; PROC. NATL. ACAD. SCI. U.S.A., BIOL. SCI.; ISSN 0273-1134; USA; DA. 1981; VOL. 78; NO 9; PP. 5833-5837; BIBL. 22 REF.Article