A WHOLE BLOOD SOLUBILITY AND CENTRIFUGATION TEST FOR SICKLE CELL HEMOGLOBIN: A CLINICAL TRIAL = UNE EPREUVE DE SOLUBILITE ET DE CENTRIFUGATION DU SANG ENTIER POUR L'EMOGLOBINE S. EXPERIMENTATION CLINIQUESERJEANT BE; SERJEANT GR.1972; AMER. J. CLIN. PATHOL.; U.S.A.; DA. 1972; VOL. 58; NO 1; PP. 11-13; BIBL. 2 REF.Serial Issue

A COMPARISON OF ERYTHROCYTE CHARACTERISTICS IN SICKLE CELL SYNDROMES IN JAMAICA = UNE COMPARAISON ENTRE LES CARACTERISTIQUES ERYTHROCYTAIRES DANS LES SYNDROMES FALCIFORMES A LA JAMAIQUESERJEANT GR; SERJEANT BE.1972; BRIT. J. HAEMATOL.; G.B.; DA. 1972; VOL. 23; NO 2; PP. 205-213; BIBL. 14REF.Serial Issue

EARLY RISE IN "PITTED" RED CELL COUNT AS A GUIDE TO SUSCEPTILITY TO INFECTION IN CHILDHOOD SICKLE CELL ANAEMIAROGERS DW; SERJEANT BE; SERJEANT GR et al.1982; ARCH. DIS. CHILD.; ISSN 0003-9888; GBR; DA. 1982; VOL. 57; NO 5; PP. 338-342; BIBL. 13 REF.Article

NEGRO ALPHA -THALASSAEMIA: GENETIC STUDIES IN HOMOZYGOUS SICKLE CELL DISEASESERJEANT GR; MASON KP; SERJEANT BE et al.1980; J. MED. GENET.; ISSN 0022-2593; GBR; DA. 1980; VOL. 17; NO 4; PP. 281-284; BIBL. 4 REF.Article

RED CELL SIZE AND THE CLINICAL AND HAEMATOLOGICAL FEATURES OF HOMOZYGOUS SICKLE CELL DISEASESERJEANT GR; FOSTER K; SERJEANT BE et al.1981; BR. J. HAEMATOL.; ISSN 0007-1048; GBR; DA. 1981; VOL. 48; NO 3; PP. 445-449; BIBL. 7 REF.Article

THE DEVELOPMENT OF HAEMOGLOBIN A₂ IN NORMAL NEGRO INFANTS AND IN SICKLE CELL DISEASESERJEANT BE; MASON KP; SERJEANT GR et al.1978; BRIT. J. HAEMATOL.; GBR; DA. 1978; VOL. 39; NO 2; PP. 259-265; BIBL. 11 REF.Article

A SIMPLE MICROMETHOD FOR THE MEASUREMENT OF FETAL HAEMOGLOBIN = UNE MICROMETHODE SIMPLE POUR LE DOSAGE L'HEMOGLOBINE FOETALESERJEANT BE; CLARKE JM; DESAI P et al.1975; J. CLIN. PATHOL.; G.B.; DA. 1975; VOL. 28; NO 9; PP. 761-764; BIBL. 16 REF.Article

CHOLELITHIASIS IN JAMAICAN PATIENTS WITH HOMOZYGOUS SICKLE CELLE DISEASE.MCCALL IW; DESAI P; SERJEANT BE et al.1977; AMER. J. HEMATOL.; U.S.A.; DA. 1977; VOL. 3; PP. 15-21; BIBL. 14 REF.Article

COMPARISON OF HAEMATOLOGICAL FEATURES OF THE BETA ⁰ AND BETA ⁺ THALASSAEMIA TRAITS IN JAMAICAN NEGROES.MILLARD DP; MASON K; SERJEANT BE et al.1977; BRIT. J. HAEMATOL.; G.B.; DA. 1977; VOL. 36; NO 2; PP. 161-170; BIBL. 1 P. 1/2Article

HEIGHTS AND WEIGHTS OF WEST INDIAN CHILDREN WITH THE SICKLE CELL TRAITASHCROFT MT; DESAI P; GRELL GAC et al.1978; ARCH. DIS. CHILDH.; GBR; DA. 1978; VOL. 53; NO 7; PP. 596-598; BIBL. 4 REF.Article

SICKLE CELL-HB LEPORE BOSTON SYNDROME. UNCOMMON DIFFERENTIAL DIAGNOSIS TO HOMOZYGOUS SICKLE CELL DISEASESTEVENS MCG; LEHMANN H; MASON KP et al.1982; AM. J. DIS. CHILD. (1960); ISSN 0002-922X; USA; DA. 1982; VOL. 136; NO 1; PP. 19-22; BIBL. 8 REF.Article

COMPARISON OF SICKLE CELL-BETA ^O THALASSAEMIA WITH HOMOZYGOUS SICKLE CELL DISEASESERJEANT GR; SOMMEREUX AM; STEVENSON M et al.1979; BRIT. J. HAEMATOL.; GBR; DA. 1979; VOL. 41; NO 1; PP. 83-93; BIBL. 14 REF.Article

HEIGHTS AND WEIGHTS OF JAMAICAN CHILDREN WITH HOMOZYGOUS SICKLE CELL DISEASE.LOWRY MF; DESAI P; ASHCROFT MT et al.1977; HUM. BIOL.; U.S.A.; DA. 1977; VOL. 49; NO 3; PP. 429-436; BIBL. 1 P.Article

THE DEVELOPMENT OF HAEMATOLOGICAL CHANGES IN HOMOZYGOUS SICKLE CELL DISEASE: A COHORT STUDY FROM BIRTH TO 6 YEARSSERJEANT GR; GRANDISON Y; LOWRIE Y et al.1981; BR. J. HAEMATOL.; ISSN 0007-1048; GBR; DA. 1981; VOL. 48; NO 4; PP. 533-543; BIBL. 4 REF.Article

HAEMOGLOBIN F VICTORIA JUBILEE (A₂^A GAMMA ₂ 80 ASP -> TYR)AHERN E; HOLDER W; AHERN V et al.1975; BIOCHIM. BIOPHYS. ACTA; PAYS-BAS; DA. 1975; VOL. 393; NO 1; PP. 188-194; BIBL. 17 REF.Article

OUTBREAK OF APLASTIC CRISES IN SICKLE CELL ANAEMIA ASSOCIATED WITH PARVOVIRUS-LIKE AGENTSERJEANT GR; MASON K; TOPLEY JM et al.1981; LANCET (BR. ED.); ISSN 0140-6736; GBR; DA. 1981; NO 8247; PP. 595-597; BIBL. 6 REF.Article

THE DETERMINANTS OF IRREVERSIBLY SICKLED CELLS IN HOMOZYGOUS SICKLE CELL DISEASESERJEANT GR; SERJEANT BE; DESAI P et al.1978; BRIT. J. HAEMATOL.; GBR; DA. 1978; VOL. 40; NO 3; PP. 431-438; BIBL. 16 REF.Article

POST-NATAL DECLINE OF FETAL HAEMOGLOBIN IN HOMOZYGOUS SICKLE CELL DISEASE: RELATIONSHIP TO PARENTAL HBF LEVELSMASON KP; GRANDISON Y; HAYES RJ et al.1982; BR. J. HAEMATOL.; ISSN 0007-1048; GBR; DA. 1982; VOL. 52; NO 3; PP. 455-463; BIBL. 1 P.Article

COAGULATION CHANGES DURING THE STEADY STATE IN HOMOZYGOUS SICKLE CELL DISEASE IN JAMAICA = (ALTERATIONS DE LA COAGULATION EN PHASE CALME DE L'ANEMIE A HEMATIES FALCIFORMES CHEZ LES HOMOZYGOTES JAMAICAINSLESLIE J; LANGLER D; SERJEANT GR et al.1975; BRIT. J. HAEMATOL.; G.B.; DA. 1975; VOL. 30; NO 2; PP. 159-166; BIBL. 26 REF.Article

Management of sickle cell disease; Lessons from the Jamaican cohort studySERJEANT, G. R; SERJEANT, B. E.Blood reviews. 1993, Vol 7, Num 3, pp 137-145, issn 0268-960XArticle

Sickle cell-hereditary persistence of fetal haemoglobin and its differentiation from other sickle cell syndromesMURRAY, N; SERJEANT, B. E; SERJEANT, G. R et al.British journal of haematology. 1988, Vol 69, Num 1, pp 89-92, issn 0007-1048Article

The emerging understanding of sickle cell diseaseSERJEANT, Graham R.British journal of haematology. 2001, Vol 112, Num 1, pp 3-18, issn 0007-1048Article

A Maqamah on Palm-Protection (Shirahah) in Arabic and Islamic Studies in Honor of Nabia Abbott IISERJEANT, R. B.Journal of Near Eastern Studies Chicago, Ill. 1981, Vol 40, Num 4, pp 307-322Article

One hundred years of sickle cell diseaseSERJEANT, Graham R.British journal of haematology. 2010, Vol 151, Num 5, pp 425-429, issn 0007-1048, 5 p.Article

Hadramawt to Zanzibar: The Pilot-Poem of the Nakhudha Said Ba Tayi of al-Hami in From Zinj to Zanzibar: Studies in History, Trade and Society on the Eastern Coast of Africa in honour of James Kirkman on the occasion of his seventy-fifth birthdaySERJEANT, R. B.Paideuma. Mitteilungen zur Kulturkunde Wiesbaden. 1982, Vol 28, pp 109-127Article