A NOTE ON THE INHERITANCE OF THE HEREDITARY PERSISTENCE OF FETAL HAEMOGLOBIN AND THE DELTA -CHAIN VARIANT HB-A₂HUISMAN THJ; GRAVELY ME; SOX R et al.1976; J. MED. GENET.; G.B.; DA. 1976; VOL. 13; NO 1; PP. 62-63; BIBL. 6 REF.Article

ALPHA-THALASSEMIA-2 AND THE VARIABILITY OF HEMATOLOGICAL VALUES IN CHILDREN WITH SICKLE CELL ANEMIAALTAY C; GRAVELY ME; JOSEPH BR et al.1981; PEDIATR. RES.; ISSN 0031-3998; USA; DA. 1981; VOL. 15; NO 8; PP. 1093-1096; BIBL. 21 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

THE SYNTHESIS OF THE ^GGAMMA AND ^AGAMMA CHAINS OF HUMAN FETAL HEMOGLOBIN IN ERYTHROID COLONIES CULTURED FROM PERIPHERAL BLOOD BFUE'S OF NORMAL ADULTS AND NEWBORN AND OF SUBJECTS WITH AN ^AGAMMA OR A G_GAMMA CHAIN ABNORMAL FETAL HEMOGLOBINHUISMAN THJ; REESE AL; GRAVELY ME et al.1980; AM. J. HEMATOL.; ISSN 0361-8609; USA; DA. 1980; VOL. 9; NO 2; PP. 137-150; BIBL. 48 REF.Article

OXYGEN EQUILIBRIUM ANALYSES OF ISOLATED HEMOGLOBINS A₂, LEPORE-WASHINGTON AND P-NILOTICRAYBOURNE SR; STALLINGS MB; GRAVELY ME et al.1978; BIOCHIM. BIOPHYS. ACTA; NLD; DA. 1978; VOL. 535; NO 1; PP. 78-84; BIBL. 14 REF.Article

THE GAMMA CHAIN HETEROGENEITY OF FETAL HEMOGLOBIN IN BLACK BETA -THALASSEMIA AND HPFH HETEROZYGOTESHUISMAN THJ; GRAVELY ME; WEBBER B et al.1981; BLOOD; ISSN 0006-4971; USA; DA. 1981; VOL. 58; NO 1; PP. 62-70; BIBL. 28 REF.Article

A NEW DELTA CHAIN VARIANT, HAEMOGLOBIN A₂-MELBOURNE OR ALPHA ₂DELTA ₂^43GLU->** (LYS(CD2))SHARMA RS; HARDING DL; WONG SC et al.1974; BIOCHEM. BIOPHYS. ACTA; PAYS-BAS; DA. 1974; VOL. 359; NO 2; PP. 233-235; BIBL. 19REF.Article

THE SYNTHESIS OF FETAL HEMOGLOBIN TYPES IN RED BLOOD CELLS AND IN BFU-E DERIVED COLONIES FROM PERIPHERAL BLOOD OF PATIENTS WITH SICKLE CELL ANEMIA, BETA ⁺- AND DELTA BETA -THALASSEMIA, VARIOUS FORMS OF HEREDITARY PERSISTENCE OF FETAL HEMOGLOBIN, NORMAL ADULTS AND NEWBORNHUISMAN THJ; EFREMOV GD; REESE AL et al.1979; HEMOGLOBIN; USA; DA. 1979; VOL. 3; NO 4; PP. 223-252; BIBL. 32 REF.Article

VARIABILITY IN THE INTERACTION OF BETA -THALASSEMIA WITH THE ALPHA -CHAIN VARIANTS HB G-PHILADELPHIA AND HB RAMPA.HUISMAN THJ; GRAVELY ME; HENSON J et al.1978; J. LAB. CLIN. MED.; USA; DA. 1978; VOL. 92; NO 2; PP. 311-320; BIBL. 24 REF.Article

HETEROZYGOSITY AND HOMOZYGOSITY FOR THE HIGH OXYGEN AFFINITY HEMOGLOBIN TARRANT OR ALPHA 126 (H9) ASP->ASN IN TWO MEXICAN FAMILIESIBARRA B; VACA G; CANTU JM et al.1981; HEMOGLOBIN; ISSN 0363-0269; USA; DA. 1981; VOL. 5; NO 4; PP. 337-348; BIBL. 12 REF.Article

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

HB P-NILOTIC IN ASSOCIATION WITH BETA ⁰-THALASSEMIA: CIS-MUTATION OF A HEMOGLOBIN BETA ^A CHAIN REGULATORY DETERMINANT.AHMED ABU SIN; FELICE AE; GRAVELY ME et al.1979; J. LAB. CLIN. MED.; USA; DA. 1979; VOL. 93; NO 6; PP. 973-982; BIBL. 16 REF.Article

HB LESLIE, AN UNSTABLE HEMOGLOBIN DUE TO DELETION OF GLUTAMINYL RESIDUE BETA 131 (H9) OCCURRING IN ASSOCIATION WITH BETA ⁰-THALASSEMIA, HBC, AND HBS.LUTCHER CL; WILSON JB; GRAVELY ME et al.1976; BLOOD; U.S.A.; DA. 1976; VOL. 47; NO 1; PP. 99-112; BIBL. 33 REF.Article