LES HEMOGLOBINES INSTABLESLABIE D; WAJCMAN H.1972; BIOCHIMIE; FR.; DA. 1972; VOL. 54; NO 5-6; PP. 625-631; ABS. ANGL.; BIBL. 17 REF.Serial Issue

MOLECULAR PATHOLOGY OF HUMAN HAEMOGLOBIN = PATHOLOGIE MOLECULAIRE DE L'HEMOGLOBINE DE L'HOMMEPERUTZ MF.1972; BIOCHIMIE; FR.; DA. 1972; VOL. 54; NO 5-6; PP. 621-622; BIBL. 6 REF.Serial Issue

THE INTERACTIONS OF SICKLE HEMOGLOBINRANNEY HM.1972; BIOCHIMIE; FR.; DA. 1972; VOL. 54; NO 5-6; PP. 633-637; ABS. FR.; BIBL. 16 REF.Serial Issue

HAEMOGLOBIN SOUTHAMPTON, BETA 106 (G8) LEU->PRO: AN UNSTABLE VARIANT PRODUCING SEVERE HAEMOLYSIS = HEMOGLOBINE SOUTHAMPTON BETA 106 (G8) LEU->PRO: UNE VARIANTE INSTABLE PRODUISANT UNE HEMOLYSE SEVEREHYDE RD; HALL MD; WILTSHIRE BG et al.1972; LANCET; G.B.; DA. 1972; NO 7788; PP. 1170-1172; BIBL. 14 REF.Serial Issue

HAEMOGLOBINOPATHIES IN AUSTRALIA = HEMOGLOBINOPATHIES EN AUSTRALIE1972; MED. J. AUSTRAL.; AUSTRAL.; DA. 1972; VOL. 59; NO 13; PP. 726-729Serial Issue

THIN-LAYER ISOELECTRIC FOCUSING FOR HAEMOGLOBIN SCREENING AND ITS APPLICATION TO HAEMOGLOBIN MALMOE = LA CONCENTRATION ISOELECTRIQUE EN COUCHE MINCE POUR LA RECHERCHE DES HEMOGLOBULINES ET SON APPLICATION A L'HEMOGLOBINE MALMOEJEPPSSON JO; BERGLUND S.1972; CLIN. CHIN. ACTA; PAYS-BAS; DA. 1972; VOL. 40; NO 1; PP. 153-158; BIBL. 1/2P.Serial Issue

Haemoglobin Warwickshire (β5[A2] Pro→Arg): a possible fine tuning of 2,3-DPG affinity by β5 ProWILSON, C. I. D; CAVE, R. J; LEHMANN, H et al.FEBS letters. 1984, Vol 176, Num 2, pp 331-333, issn 0014-5793Article

A new hemoglobin with high oxygen affinity-hemoglobin bunbury: α₂β₂ [94(FG1) Asp→Asn]COMO, P. F; KENNETT, D; WILKINSON, T et al.Hemoglobin. 1983, Vol 7, Num 5, pp 413-421, issn 0363-0269Article

Hemoglobin maputo: a new β-chain variant (α₂β₂ 47 (CD6) Asp→Tyr) in combination with hemoglobin S, identified by high performance liquid chromatography (HPLC)MARINUCCI, M; BOISSEL, J. P; MASSA, A et al.Hemoglobin. 1983, Vol 7, Num 5, pp 423-433, issn 0363-0269Article

Hemoglobin Minneapolis-Laos [β-118 (GH1) Phe→Tyr] a new hemoglobin variant with normal functional propertiesMORRISON, W. T; ADAMS, J. III.Hemoglobin. 1984, Vol 8, Num 1, pp 75-78, issn 0363-0269Article

A single-base change at a splice site in a β°-thalassemic gene causes abnormal RNA splicingTREISMAN, R; PROUDFOOT, N. J; SHANDER, M et al.Cell (Cambridge). 1982, Vol 29, Num 3, pp 903-911, issn 0092-8674Article

Antenatal diagnosis of haemoglobinopathies by improved method of isoelectric focusing of haemoglobinsFERRARI, M; CREMA, A; CANTU-RAJNOLDI, A et al.British journal of haematology. 1984, Vol 57, Num 2, pp 265-270, issn 0007-1048Article

HB F-Yamaguchi (γ75THR, γ80ASN, γ136ALA) is associated with ^Gγ-thalassemiaNAKATSUJI, T; OHBA, Y; HUISMAN, T. H. J et al.American journal of hematology. 1984, Vol 16, Num 2, pp 189-192, issn 0361-8609Article

Hemoglobin Köln: analysis of linkage relationships between the mutant gene and polymorphic restriction sites in the β-globin gene clusterHORST, J; OEHME, R; KLEIHAUER, E et al.Blut. 1984, Vol 48, Num 4, pp 213-219, issn 0006-5242Article

Hemoglobin quin-hai, β78(EF2) Leu→Arg, a new abnormal hemoglobin found in Guangdong, ChinaPONG CHEH JEN; CHEN, L. C; CHEN, P. F et al.Hemoglobin. 1983, Vol 7, Num 5, pp 407-412, issn 0363-0269Article

HB St. Luke's [α95(G2) Pro→Arg] in JapanHARANO, T; HARANO, K; SHIBATA, S et al.Hemoglobin. 1983, Vol 7, Num 5, pp 471-472, issn 0363-0269Article

Hemoglobin chad [α23(B4) Glu→Lys] discovered in a japanese with questionable polycythemiaHARANO, T; HARANO, K; SHIBATA, S et al.Hemoglobin. 1983, Vol 7, Num 6, pp 581-584, issn 0363-0269Article

HB J Oxford [α15 (A13) Gly → Asp] in JapanHARANO, K; HARANO, T; SHIBATA, S et al.Hemoglobin. 1984, Vol 8, Num 2, pp 197-198, issn 0363-0269Article

A silent, neutral substitution detected by reverse-phase high-performance liquid chromatography: hemoglobin BeirutSTRAHLER, J. R; ROSENBLOOM, B. B; HANASH, S. M et al.Science (Washington, D.C.). 1983, Vol 221, Num 4613, pp 860-863, issn 0036-8075Article

Hemoglobin J lome: β59(E3) lysine→asparagine observed in a japanese familySUGIHARA, J; NAKASHIMA, H; YOKOTA, E et al.Hemoglobin. 1983, Vol 7, Num 6, pp 585-589, issn 0363-0269Article

The δβ crossover region in Lepore Boston hemoglobinopathy is restricted to a 59 base pairs region around the 5' splice junction of the large globin gene intervening sequenceMAVILIO, F; GIAMPAOLO, A; CARE, A et al.Blood. 1983, Vol 62, Num 1, pp 230-233, issn 0006-4971Article

RELIABLE ROUTINE ESTIMATION OF SMALL AMOUNTS OF FOETAL HAEMOGLOBIN BY ALKALI DENATURATION = METHODE INTERESSANTE POUR L'EVALUATION COURANTE DE FAIBLES QUANTITES D'HEMOGLOBINE FOETALE PAR DENATURATION ALCALINEPEMBREY ME; MCWADE P; WEATHERALL DJ et al.1972; J. CLIN. PATHOL.; G.B.; DA. 1972; VOL. 25; NO 8; PP. 738-740; BIBL. 9REF.Serial Issue

HEMOGLOBIN G SASKATOON IN ASSOCIATION WITH PHN IN AN IRANIAN SOLDIERNIAZI GA; ZAMANIANPOOR M; ALA F et al.1981; HEMOGLOBIN; USA; DA. 1981; VOL. 5; NO 1; PP. 85-87; BIBL. 14 REF.Article

PREFERENTIAL BINDING OF BETA ^C RELATIVE TO BETA ^S GLOBIN TO STROMA IN HEMOGLOBIN SC DISEASENATTA C; MUIR M.1980; HEMOGLOBIN; USA; DA. 1980; VOL. 4; NO 2; PP. 157-163; BIBL. 9 REF.Article

BETA ⁰-THALASSEMIA IN ASSOCIATION WITH HB LESLIE (ALPHA ₂BETA ₂ 131GLN->0) IN A SARDINIAN FAMILYCARCASSI UEF; PINTUS A; GRAVELY ME et al.1980; HEMOGLOBIN; USA; DA. 1980; VOL. 4; NO 2; PP. 195-200; BIBL. 7 REF.Article