International Hemoglobin Information Center variants list.

No abstract is available for this paper.

• Publication year

  1991

• Venue

  Hemoglobin

• Publication date

  Unknown publication date

• Fields of study

  Medicine

• Identifiers
  PMID 2061092
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• Hb Cordele alpha(2)47 (CE5)Asp----Ala beta 2. A mildly unstable variant observed in black twins.

  2009cited by this paper
• Hemoglobin Atago (alpha2-85Tyr beta-2) a new abnormal human hemoglobin found in Nagasaki. Biochemical studies on hemoglobins and myoglobins. VI.

  2009cited by this paper
• Haemoglobin M Saskatoon and haemoglobin M Hyde Park in two Yugoslavian families.

  2009cited by this paper
• Hemoglobin Cagliari (beta 60 [E4] Val----Glu): a novel unstable thalassemic hemoglobinopathy.

  1991cited by this paper
• Hemoglobin Montreal: a new variant with an extended beta chain due to a deletion of Asp, Gly, Leu at positions 73, 74, and 75, and an insertion of Ala, Arg, Cys, Gln at the same location.

  1991cited by this paper
• Hb F-Brooklyn or alpha 2G gamma 2(66)(E10)Lys----Gln.

  1990cited by this paper
• [Structural analysis of abnormal hemoglobin by the polymerase chain reaction (PCR) of genomic DNA].

  1990cited by this paper
• A new slow-moving hemoglobin variant Hb Tianshui or alpha 2 beta(2)39(C5)Gln----Arg, observed in a Chinese family living in Gansu.

  1990cited by this paper
• Hb Johnstown [beta 109 (G11) Val----Leu]: a new electrophoretically silent variant that causes erythrocytosis.

  1990cited by this paper
• Hb J-Anatolia [alpha 61(E10)Lys----Thr]: structural characterization and gene localization of a new alpha chain variant.

  1990cited by this paper
• Hemoglobin Calais [beta 76 (E20) Ala----Pro]: a hemoglobin variant with decreased intrinsic oxygen affinity.

  1990cited by this paper
• Hb F-Jiangsu, the first gamma chain variant with a valine----methionine substitution: alpha 2A gamma 2 134(H12)Val----Met.

  1990cited by this paper
• New results of hemoglobin variant structure determinations by fast atom bombardment mass spectrometry.

  1990cited by this paper
• Characterization of Hb Aalborg, a new unstable hemoglobin variant, by fast atom bombardment mass spectrometry.

  1990cited by this paper
• Hb Yamagata [beta 132(H10)Lys----Asn]: a new abnormal hemoglobin in a Japanese family.

  1990cited by this paper
• Hemoglobin Warsaw (Phe beta 42(CD1)----Val), an unstable variant with decreased oxygen affinity. Characterization of its synthesis, functional properties, and structure.

  1990cited by this paper
• Hb Fukuoka [beta 2(NA2)His----Tyr]: a new mutation at the 2,3-diphosphoglycerate binding site.

  1990cited by this paper
• Hb Matera [beta 55(D6)Met----Lys]: a new unstable hemoglobin variant in an Italian family.

  1990cited by this paper
• Hb Sun Prairie or alpha(2)130(H13)Ala----Pro beta 2, a new unstable variant occurring in low quantities.

  1990cited by this paper
• Structural, functional, and subunit assembly properties of hemoglobin Attleboro [alpha 138 (H21) Ser----Pro], a variant possessing a site maturation at a critical C-terminal residue.

  1990cited by this paper
• A new alpha chain variant Hb Tonosho [alpha 110(G17)Ala----Thr]: subunit dissociation during cation exchange chromatography for Hb A1c assay.

  1990cited by this paper
• Hemoglobin Birmingham and hemoglobin Galicia: two unstable beta chain variants characterized by small deletions and insertions.

  1990cited by this paper
• Hb Zengcheng or alpha 2 beta(2)114(G16)Leu----Met.

  1990cited by this paper
• Hb Iowa or alpha 2 beta 2(119)(GH2)Gly----Ala.

  1990cited by this paper
• Hb Fukutomi [alpha 126(H9)Asp----Val]: a new hemoglobin variant with high oxygen affinity.

  1990cited by this paper
• Hb Sun Prairie or alpha(2)130(H13)Ala----Pro beta 2; second observation in an Indian adult.

  1990cited by this paper
• Hemoglobin Dhonburi alpha 2 beta 2 126 (H4) Val----Gly: a new unstable beta variant producing a beta-thalassemia intermedia phenotype in association with beta zero-thalassemia.

  1990cited by this paper
• Hb F-Catalonia or alpha 2G gamma(2)15(A12)Trp----Arg.

  1990cited by this paper
• Hemoglobin Nevers [alpha 2 beta 2130(H8)Tyr----Ser]; a new silent variant found in France.

  1990cited by this paper
• A new hemoglobin variant found during investigations of diabetes mellitus: Hb Pavie [alpha 135 (H18) Val----Glu].

  1990cited by this paper
• Hb F-Onoda or alpha 2G gamma 2(146)(HC3)His----Tyr, a newly discovered fetal hemoglobin variant in a Japanese newborn.

  1990cited by this paper
• Hemoglobin FM-Fort Ripley: another lesson from the neonate.

  1989cited by this paper
• Hb Fontainebleau [alpha 21(B2)Ala----pro], a new silent mutant hemoglobin.

  1989cited by this paper
• Hb Masuda [beta 114(G16)Leu----Met, 119(GH2)Gly----Asp], a hemoglobin with two substitutions in the beta chain.

  1989cited by this paper
• Hb Hinsdale [beta 139 (H17)Asn----Lys]: a variant in the central cavity showing reduced affinity for oxygen and 2,3-diphosphoglycerate.

  1989cited by this paper
• Hb Moriguchi or alpha 2 beta 2(97) (FG4)His---Tyr substitution at the alpha 1-beta 2 interface.

  1989cited by this paper
• Hemoglobin Villejuif [beta 123(H1) Thr----Ile]: a new variant found in coincidence with polycythemia vera.

  1989cited by this paper
• Hb Gainesville-GA or alpha 2 beta 2(46)(CD5)Gly----Arg; second report.

  1989cited by this paper
• A 5' splice-region G----C mutation in exon 1 of the human beta-globin gene inhibits pre-mRNA splicing: a mechanism for beta+-thalassemia.

  1989cited by this paper
• Mutant fetal hemoglobin causing cyanosis in a newborn.

  1989cited by this paper
• Hb N-Timone [alpha 2 beta 2(8)(A5)Lys----Glu]: a new fast-moving variant with normal stability and oxygen affinity.

  1989cited by this paper
• Hb Extremadura or alpha 2 beta 2133 (H11)Val----Leu, a new mildly unstable hemoglobin in a Spanish female.

  1989cited by this paper
• Hb Chad or alpha 223(B4)Glu----Lys beta 2 observed in members of a Surinam family in association with alpha-thalassemia-2 and with Hb S.

  1989cited by this paper
• Some abnormal hemoglobin identifications in the U.S.S.R. by micropreparative thin layer peptide mapping.

  1989cited by this paper
• Hb Belliard [alpha 56(E5)Lys----Asn] a new fast-moving alpha chain variant found in a subject of Spanish origin.

  1989cited by this paper
• Hemoglobin Nouakchott [alpha 114(GH2)Pro----Leu]: a new hemoglobin variant displaying an unusual increase in hydrophobicity.

  1989cited by this paper
• Hb Brockton [alpha 2 beta 2138(H16)Ala----Pro] observed in a Turkish girl.

  1989cited by this paper
• Hb Reims [alpha 2(23)(B4)Glu----Gly beta 2]: a new alpha chain variant with slightly decreased stability.

  1989cited by this paper
• Hb A2-Wrens or alpha 2 delta 2 98(FG5) Val----Met, an unstable delta chain variant identified by sequence analysis of amplified DNA.

  1989cited by this paper
• Hb Monroe or alpha 2 beta 230(B12)Arg----Thr, a variant associated with beta-thalassemia due to A G----C substitution adjacent to the donor splice site of the first intron.

  1989cited by this paper
• Hemoglobin Windsor or beta 11 (A8)Val----Asp: a new unstable beta-chain hemoglobin variant producing a hemolytic anemia.

  1989cited by this paper
• Hb Himeji or alpha 2 beta 2(140)(H18)Ala----Asp in a Portuguese family.

  1989cited by this paper
• Hb Luxembourg [alpha 24(B5) Tyr----His]: a new unstable variant.

  1989cited by this paper
• Hb F-Fukuyama or A gamma T43(CD2)Asp----Asn.

  1989cited by this paper
• Hb Miyano or alpha 41(C6)Thr----Ser: a new high oxygen affinity alpha chain variant found in an erythremic blood donor.

  1989cited by this paper
• Hb Warsaw (β42 Phe → Val): An unstable hemoglobin with decreased oxygen affinity. I. Hematologic and clinical expression

  1989cited by this paper
• Hb Bruxelles: alpha 2A beta (2)41 or 42(C7 or CD1)Phe deleted.

  1989cited by this paper
• A NEW DOUBLY SUBSTITUTED SICKLING HAEMOGLOBIN: HbS‐OMAN

  1989cited by this paper
• Hb Catonsville (glutamic acid inserted between Pro-37(C2)alpha and Thr-38(C3)alpha). Nonallelic gene conversion in the globin system?

  1989cited by this paper
• Molecular characterization of beta-globin gene mutations in Malay patients with Hb E-beta-thalassaemia and thalassaemia major.

  1989cited by this paper
• Hb Chandigarh or alpha 2 beta 2(94)(FG1)Asp----Gly observed in an Indian family.

  1989cited by this paper
• Hb Evans or alpha 262(E11)Val----Met beta 2; an unstable hemoglobin causing a mild hemolytic anemia.

  1989cited by this paper
• Hemoglobin hafnia: alpha 2 (beta 116 (G18) His----Gln)2; a new hemoglobin variant mistaken for glycated hemoglobin.

  1988cited by this paper
• Hb Tunis [alpha 2 beta 2 124 (H2)Pro----Ser], a new beta chain variant identified by HPLC.

  1988cited by this paper
• Hb F-Austell or alpha 2G gamma (2)40(C6)Arg----Lys.

  1988cited by this paper
• Hemoglobin Brest [beta 127 (H5)Gln----Lys] a new unstable human hemoglobin variant located at the alpha 1 beta 1 interface with specific electrophoretic behavior.

  1988cited by this paper
• Hemoglobin Saverne: a new variant with elongated beta chains: structural and functional properties.

  1988cited by this paper
• An electrophoretically silent hemoglobin variant, Hb Hekinan [alpha 27(B8)Glu----Asp] found in a Japanese.

  1988cited by this paper
• Hb Le Lamentin or alpha 2 20(B1)His----GLN beta 2 found in a Spanish family.

  1988cited by this paper
• Hb natal or alpha 2(minus Tyr-Arg) beta 2: a high oxygen affinity alpha chain variant with a deleted carboxy-terminus resulting from a TAC----TAA (Tyr----terminating codon) mutation in codon alpha 140.

  1988cited by this paper
• Hyperunstable hemoglobin Koriyama anti-Hb Gun Hill insertion of five residues in the beta chain.

  1988cited by this paper
• Hb Fukuyama [beta 77(EF1)His----Tyr]: a new abnormal hemoglobin discovered in a Japanese.

  1988cited by this paper
• Hb F-Granada or alpha 2G gamma (2)22(B4)Asp----Val: a new human fetal hemoglobin variant.

  1988cited by this paper
• Hb J-Cordoba [alpha 2A beta 2(95)(FG2)Lys----Met]. A new Hb variant found in Argentina.

  1988cited by this paper
• Hb A‐LIKE SICKLE HAEMOGLOBIN: Hb S‐PROVIDENCE

  1988cited by this paper
• Hemoglobin Brockton [beta 138 (H16) Ala----Pro]: an unstable variant near the C-terminus of the beta-subunits with normal oxygen-binding properties.

  1988cited by this paper
• Some rare hemoglobin variants with altered oxygen affinities; Hb linkoping [beta 36(C2)Pro----Thr], Hb Caribbean [beta 91(F7)Leu----Arg], and Hb Sunnybrook [beta 36(C2)Pro----Arg].

  1988cited by this paper
• Increased oxygen affinity with normal heterotropic effects in hemoglobin Loire [alpha 88(F9)Ala----Ser].

  1988cited by this paper
• Hemoglobin Tilburg: alpha 2-beta 2 73 (E 17) Asp----Gly. A new hemoglobin with reduced oxygen affinity.

  1988cited by this paper
• Hb Las Palmas or alpha 2 beta 2(49)(CD8)Ser----Phe, a mildly unstable hemoglobin variant.

  1988cited by this paper
• Hb F-Baskent or alpha 2A gamma 128(H6)Ala----Thr.

  1988cited by this paper
• Hemoglobin Pierre-Bénite [beta 90(F6)Glu----Asp], a new high affinity variant found in a French family.

  1988cited by this paper
• Hemoglobin Randwick or beta 15 (A12)Trp----Gly: a new unstable beta-chain hemoglobin variant.

  1988cited by this paper
• A new unstable haemoglobin variant: Hb Shanghai [beta 131(H9)Gln----Pro] found in China.

  1987cited by this paper
• A new unstable and low oxygen affinity hemoglobin variant: Hb J-Auckland [beta 25(B7)Gly----Asp].

  1987cited by this paper
• Hb J-Pontoise or alpha 2(63)(E12)Ala----Asp beta 2 in four members of a Spanish family.

  1987cited by this paper
• Hb F-Oakland or alpha 2G gamma I2(26)(B8)Glu----Lys.

  1987cited by this paper
• Hb F-Xinjiang or A gamma T25(B7)Gly----Arg: a new slow-moving unstable fetal hemoglobin variant.

  1987cited by this paper
• Hb Olomouc or alpha 2 beta 2(86)(F2)Ala----Asp, a new high oxygen affinity variant.

  1987cited by this paper
• Hemoglobin Hangzhou alpha 64(E13)Asp----Gly. A new variant found in China.

  1987cited by this paper
• Hemoglobin Grange‐Blanche [β27(B9) Ala → Val], a new variant with normal expression and increased affinity for oxygen

  1987cited by this paper
• Hb F-Xin-Su or A gamma I73(E17)Asp----His: a new slow-moving fetal hemoglobin variant.

  1987cited by this paper
• Hemoglobin Chico [beta 66(E10)Lys----Thr]: a new variant with decreased oxygen affinity.

  1987cited by this paper
• A novel globin structural mutant, Showa-Yakushiji (beta 110 Leu-Pro) causing a beta-thalassemia phenotype.

  1987cited by this paper
• [Hemoglobin Boumerdès alpha 2(37) (C2) Pro----Arg beta 2: a new variant of the alpha chain associated with hemoglobin S in an Algerian family].

  1987cited by this paper
• Hemoglobin I High Wycombe in an Australian family.

  1987cited by this paper
• Hb Sassari or alpha (2)126(H9)Asp---His beta 2 observed in a family from Northern Sardinia.

  1987cited by this paper
• Hb D-Granada or alpha 2 beta 2 22(B4)Glu----Val.

  1987cited by this paper
• Structure and function of a new hemoglobin variant, Hb meilahti (alpha 2 beta 2 36(C2)Pro----Thr), characterized by mass spectrometry.

  1987cited by this paper
• Hb F-Clarke or alpha 2G gamma 2(65)(E9)Lys----Asn.

  1987cited by this paper

• Rapid detection of point mutations and polymorphisms of the alpha-globin genes by DGGE and SSCA.

  1996cites this paper
• Hemoglobin Ozieri: a new alpha-chain variant (alpha 71(E20)Ala-->Val). Characterization using FAB- and electrospray-mass spectrometric techniques.

  1993cites this paper
• Recombinant haemoglobin in the development of red-blood-cell substitutes.

  1992cites this paper
• Hb Olomouc [alpha 2 beta 2(86)(F2)Ala----Asp] found in a Japanese family.

  1992cites this paper
• A new alpha chain variant, Hb Hanamaki or alpha 2(139)(HC1)Lys----Glu beta 2, found in a Japanese family.

  1992cites this paper
• Hb Kodaira [beta 146(HC3)His----Gln]: a new beta chain variant with an amino acid substitution at the C-terminus.

  1992cites this paper
• Two new human hemoglobin variants caused by unusual mutational events: Hb Zaïre contains a five residue repetition within the α-chain and Hb Duino has two residues substituted in the β-chain

  1992cites this paper
• Rapid molecular diagnosis of hemoglobin variants by RT-PCR of reticulocyte mRNA and direct sequencing.

  1992cites this paper
• Hb Kanagawa [alpha 40(C5)Lys----Met]: a new alpha chain variant with an increased oxygen affinity.

  1992cites this paper
• Association of Hb Hope [beta 136(H14)Gly----Asp] and alpha-thalassemia-2 (3.7 Kb deletion) causing severe microcytic anemia.

  1992cites this paper
• Hb F-Xinjiang or alpha 2A gamma T(2)25(B7)Gly----Arg identified by reversed phase HPLC; second observation.

  1991cites this paper
• Gamma chain abnormalities and gamma-globin gene rearrangements in newborn babies of various populations.

  1991cites this paper
• Hb Coimbra or alpha 2 beta (2)99(G1)Asp----Glu, a newly discovered highoxygen affinity variant.

  1991cites this paper