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TWO FAMILIES WITH HAEMOGLOBINOPATHIES RARELY OBSERVED IN ITALY (HBC AND HBDPI UNJAB CONTIENT = DEUX FAMILLES PRESENTANT UNE HEMOGLOBINOPATHIE RAREMENT OBSERVEE EN ITALIE (HBC ET HBDPI UNJAB CONTIENT LAMEDICA GM; LAMEDICA G; CERRUTI MAINARDI P et al.1972; PANMINERVA MED.; ITAL.; DA. 1972; VOL. 14; NO 9; PP. 270-275; BIBL. 28 REF.Serial Issue

GLOBIN CHAIN SYNTHESIS IN THE MARROW AND RETICULOCYTES OF BETA THALASSEMIA, HEMOGLOBIN H DISEASE, AND BETA DELTA THALASSEMIA = SYNTHESE DES CHAINES DE GLOBINE DANS LA MOELLE ET LES RETICULOCYTES AU COURS DE LA BETA THALASSEMIE, DE L'HEMOGLOBINOSE H ET DE LA BETA DELTA THALASSEMIESHCHORY M; RAMOT B.1972; BLOOD; U.S.A.; DA. 1972; VOL. 40; NO 1; PP. 105-111; BIBL. 21REF.Serial Issue

HUMAN GLOBIN GENE ANALYSIS FOR A PATIENT WITH BETA O/DELTA BETA O-THALASSEMIAOTTOLENGHI S; LANYON WG; WILLIAMSON R et al.1975; PROC. NATION. ACAD. SCI. U.S.A.; U.S.A.; DA. 1975; VOL. 72; NO 6; PP. 2294-2299; BIBL. 30 REF.Article

EARLY SPLENECTOMY IN THE MANAGEMENT OF THALASSEMIC CHILDREN IN DJAKARTA = SPLENECTOMIE PRECOCE DANS LE TRAITEMENT DE LA THALASSEMIE CHEZ LES ENFANTS A DJAKARTAWAHIDIJAT I; MARKUM AH; ADANG ZK et al.1972; ACTA HAEMATOL.; SUISSE; DA. 1972; VOL. 48; NO 1; PP. 28-33; BIBL. 20REF.Serial Issue

DOUBLE HETEROZYGOUS BETA DELTA -THALASSEMIA IN NEGROES = THALASSEMIE BETA DELTA BI-HETEROZYGOTE CHEZ DES NOIRSZELKOWITZ L; TORRES C; BHOOPALAM N et al.1972; ARCH. INTERN. MED.; U.S.A.; DA. 1972; VOL. 129; NO 6; PP. 975-979; BIBL. 30REF.Serial Issue

THE BETA THALASSAEMIASFESSAS P; LOUKOPOULOS D.1974; CLIN. IN HAEMATOL.; G.B.; DA. 1974; VOL. 3; NO 2; PP. 411-435; BIBL. 2P.1/2Article

A CASE OF HAEMOGLOBIN J SARDEGNA/BETA -THALASSAEMIA DOUBLE HETEROZYGOSIS = UN CAS DE DOUBLE HETEROZYGOTIE D'HEMOGLOBINE J SARDEGNA/BETA -THALASSEMIEGALLO E; PUGLIATTI L; RICCO G et al.1972; ACTA HAEMATOL.; SUISSE; DA. 1972; VOL. 47; NO 5; PP. 311-320; BIBL. 26REF.Serial Issue

ABNORMAL OR ABSENT BETA MRNA IN BO FERRARA AND GENE DELETION IN DELTA BETA THALASSAEMIA.RAMIREZ F; O'DONNELL JV; MARKS PA et al.1976; NATURE; G.B.; DA. 1976; VOL. 263; NO 5577; PP. 471-475; BIBL. 25 REF.Article

BETA O THALASSAEMIA. TIME FOR A REAPPRAISAL. = BETA O THALASSEMIE. REAPPRECIATION DE CETTE MALADIECLEGG JB; WEATHERALL DJ.1974; LANCET; G.B.; DA. 1974; NO 7873; PP. 133-135; BIBL. 22REF.Article

GENERALIDADES SOBRE LOS SINDROMES BETA-TALASEMICOS = GENERALITES SUR LES SYNDROMES BETA -THALASSEMIQUESSAENZ GF.1976; SANGRE; ESP.; DA. 1976; VOL. 21; NO 1; PP. 157-163; BIBL. 33 REF.Article

LES BETA-THALASSEMIESTALEB N.1972; VIE MED. CANADA FR.; CANADA; DA. 1972; VOL. 1; NO 5; PP. 478-490; BIBL. 3P.Serial Issue

THE ASSOCIATION OF SICKLE CELL ANEMIA WITH HETEROZYGOUS AND HOMOZYGOUS ALPHA -THALASSEMIA-2: IN VITRO HB CHAIN SYNTHESISFELICE AE; WEBBER B; MILLER A et al.1979; AMER. J. HEMATOL.; USA; DA. 1979; VOL. 6; NO 2; PP. 91-106; BIBL. 30 REF.Article

I PRINCIPALI PARAMETRI EMATOLOGICI NEI PORTATORI ADULTI DI BETA -TALASSEMIA = LES PRINCIPAUX PARAMETRES HEMATOLOGIQUES CHEZ LES PORTEURS ADULTES DE BETA-THALASSEMIEZANNOTTI M; MARTUZZI VERONESI F; FAVERO A et al.1975; TRASFUS. DEL SANGUE; ITAL.; DA. 1975; VOL. 20; NO 1; PP. 33-40; ABS. FR. ANGL. ESP.; BIBL. 3REF.Article

HAEMOGLOBIN SYNTHESIS DURING ERYTHROID MATURATION IN BETA -THALASSAEMIACLEGG JB; WEATHERALL DJ.1972; NATURE NEW BIOL.; G.B.; DA. 1972; VOL. 204; NO 101; PP. 190-192; BIBL. 12REF.Serial Issue

GLOBIN CHAIN SYNTHESIS IN VARIOUS ANEMIASRAMOT B; SHCHORY M; MOZEL M et al.1972; BIOCHIMIE; FR.; DA. 1972; VOL. 54; NO 5-6; PP. 669-673; ABS. FR.; BIBL. 11 REF.Serial Issue

UNUSUAL COMBINATION OF GENETIC DEFECTS IN A SILICIAN BOY: GGAMMA AGAMMA DELTA BETA THALASSEMIA, GGAMMA AGAMMA HETEROCELLULAR HPFH, BETA O THALASSEMIA, AND ALBINISMSCHILIRO G; PAVONE L; ROMEO MA et al.1983; AMERICAN JOURNAL OF MEDICAL GENETICS; ISSN 0148-7299; USA; DA. 1983; VOL. 15; NO 2; PP. 225-231; BIBL. 20 REF.Article

HAEMOGLOBIN Q INDIA (ALPHA 64 (E13) ASPARTIC ACID->HISTIDINE) ASSOCIATED WITH BETA -THALASSAEMIA OBSERVED IN THREE SINDHI FAMILIES = HEMOGLOBINE Q INDIA (ALPHA 64 (E13) ACIDE ASPARTIQUE->HISTIDINE) ASSOCIEE A UNE BETA -THALASSEMIE DANS TROIS FAMILLES SINDHISUKUMARAN PK; MERCHANT SM; DESAI MP et al.1972; J. MED. GENET.; G.B.; DA. 1972; VOL. 9; NO 4; PP. 436-442; BIBL. 17REF.Serial Issue

PARTICULARITES DES TROUBLES VASCULO-CEREBRAUX CHEZ LES ENFANTS ATTEINTS DE THALASSEMIE BETA MAJEUREMUTALIMOVA AB.1975; ZH. NEUROPATOL. PSIKHIATR. S.S. KORSAKOVA; S.S.S.R.; DA. 1975; VOL. 75; NO 10; PP. 1484-1489; ABS. ANGL.; BIBL. 32 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

NORMAL AND ABNORMAL HUMAN HEMOGLOBINS1972; ADV. CLIN. CHEM.; U.S.A.; DA. 1972; VOL. 15; PP. 149-253; BIBL. 29P.Serial Issue

POPULATION SCREENING FOR BETA -THALASSAEMIAFLATZ SD; FLATZ G.1980; LANCET (BR. ED.); ISSN 0140-6736; GBR; DA. 1980; NO 8193; PP. 495-496; BIBL. 6 REF.Article

SERUM LIPID PEROXIDATION IN BETA -THALASSAEMIAMAGGIONI G; MURGIA F; CORRADO G et al.1978; HAEMATOLOGICA; ITA; DA. 1978; VOL. 63; NO 3; PP. 338-339; BIBL. 10 REF.Article

STUDY OF A LARGE ANGLO-SAXON FAMILY WITH BETA -THALASSAEMIA TRAIT = ETUDE D'UNE GRANDE FAMILLE ANGLO-SAXONE PRESENTANT UN TRAIT BETA -THALASSEMIQUERAIK E; POWELL E; GORDON S et al.1976; ACTA HAEMATOL.; SUISSE; DA. 1976; VOL. 55; NO 1; PP. 40-47; BIBL. 6 REF.Article

THE OXYGEN AFFINITY OF HAEMOGLOBIN EMAY A; HUEHNS ER.1975; BRIT. J. HAEMATOL.; G.B.; DA. 1975; VOL. 30; NO 2; PP. 177-184; BIBL. 8REF.Article

APPEARANCE OF BETA -GLOBIN SYNTHESIS IN ERYTHROID CELLS OF FERRARA BETA O-THALASSAEMIC PATIENTS FOLLOWING BLOOD TRANSFUSION = APPARITION D'UNE SYNTHESE DE BETA -GLOBINE DANS LES CELLULES ERYTHROIDES DE SUJETS ATTEINTS DE THALASSEMIE BETA -FERRARA APRES UNE TRANSFUSION SANGUINECONCONI F; DEL SENNO L; FERRARESE P et al.1975; NATURE; G.B.; DA. 1975; VOL. 254; NO 5497; PP. 256-259; BIBL. 13REF.Article

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