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4. Mapping the alpha-globin genes in Hb J Mexico carriers. Trabuchet G; Morle F; Verdier G; Godet J; Benabadji M; Nigon VM Hum Genet; 1982; 62(2):164-6. PubMed ID: 6298095 [TBL] [Abstract][Full Text] [Related]
5. Atypical hemoglobin H disease in a Thai patient resulting from a combination of alpha-thalassemia 1 and hemoglobin Constant Spring with hemoglobin J Bangkok heterozygosity. Fucharoen S; Ayukarn K; Sanchaisuriya K; Fucharoen G Eur J Haematol; 2001 May; 66(5):312-6. PubMed ID: 11422410 [TBL] [Abstract][Full Text] [Related]
6. Haemoglobin J Rovigo 53 alpha (E-2) aspartic acid alanin. Araujo JT; Plowman D; Araujo RA; de Souza LF; Lehmann H Rev Bras Pesqui Med Biol; 1980 Apr; 13(1-3):37-9. PubMed ID: 7414024 [TBL] [Abstract][Full Text] [Related]
7. A Hb J Cape Town homozygote--association of Hb J Cape Town and alpha-thalassaemia. Botha MC; Stathopoulou R; Lehmann H; Rees JS; Plowman D FEBS Lett; 1978 Dec; 96(2):331-4. PubMed ID: 729801 [No Abstract] [Full Text] [Related]
8. Hb J-Meerut [alpha 120(H3)Ala----Glu] found in a Japanese family. Harano T; Harano K; Imai K; Yunoki H; Yagi H; Nagashima K; Kuroume T Hemoglobin; 1989; 13(2):169-75. PubMed ID: 2737912 [No Abstract] [Full Text] [Related]
9. Hb N-Baltimore [alpha 2 beta 2(95)(FG2)Lys----Glu] and Hb J-Iran [alpha 2 beta 2(77)(Ef1]His----Asp] observed in a Turkish family from Antalya. Bircan I; Güven AG; Yegin O; Plaseska D; Wilson JB; Ramachandran M; Huisman TH Hemoglobin; 1990; 14(4):453-7. PubMed ID: 2283300 [No Abstract] [Full Text] [Related]
10. Genetic and biosynthetic studies of families carrying hemoglobin J alpha Mexico: association of alpha-thalassemia with HbJ. Trabuchet G; Benabadji M; Labie D Hum Genet; 1978 Jun; 42(2):189-99. PubMed ID: 669703 [TBL] [Abstract][Full Text] [Related]
11. Occurrence of haemoglobin Norfolk (alpha2 57 (E6) Gly leads to Asp beta2) at the level of 33% in an Italian family from Calabria. Marinucci M; Mavilio F; Samoggia P; Tentori L; Spadea G; Cocone G Acta Haematol; 1979; 61(1):39-46. PubMed ID: 105539 [TBL] [Abstract][Full Text] [Related]
12. Hemoglobin I (alpha 16(A14) Lys replaced by Glu) and hemoglobin J Iran (beta 77(EF1) His replaced by Asp) discovered in Japanese. Saito S; Fujita S; Ohta Y; Kobayashi Y Hemoglobin; 1982; 6(5):537-41. PubMed ID: 6129205 [No Abstract] [Full Text] [Related]
13. Proportion of hemoglobin G Philadelphia (alpha 268 Asn leads to Lys beta 2) in heterozygotes is determined by alpha-globin gene deletions. Sancar GB; Tatsis B; Cedeno MM; Rieder RF Proc Natl Acad Sci U S A; 1980 Nov; 77(11):6874-8. PubMed ID: 6935689 [TBL] [Abstract][Full Text] [Related]
14. Studies on a family with Hb J Calabria (alpha 2 beta 2 64 (E8) Gly replaced by Asp). Marinucci M; Mavilio F; Fontanarosa PP; Tentori L; Brancati C Hemoglobin; 1979; 3(5):327-40. PubMed ID: 500375 [TBL] [Abstract][Full Text] [Related]
15. Australian beta zero-thalassaemia: a high haemoglobin A2 beta zero-thalassaemia due to a 12 kb deletion commencing 5' to the beta-globin gene. Motum PI; Lindeman R; Hamilton TJ; Trent RJ Br J Haematol; 1992 Sep; 82(1):107-13. PubMed ID: 1419783 [TBL] [Abstract][Full Text] [Related]
16. Double heterozygosis for Hb J Paris and beta-thalassemia. Marinucci M; Bruni E; Tentori L; De Sandre G; Vettore L Hemoglobin; 1977; 1(6):595-8. PubMed ID: 914639 [No Abstract] [Full Text] [Related]
17. Hb Strumica [alpha(2)112(G19)His----Arg beta 2] in a Turkish family. Akar N; Arcasoy A; Ata Y Hemoglobin; 1991; 15(4):347-8. PubMed ID: 1787106 [No Abstract] [Full Text] [Related]
18. Hb J-Calabria [beta 64(E8)Gly----Asp] found in a Japanese family. Harano T; Harano K; Imai K; Ohnishi T; Akabori T Hemoglobin; 1989; 13(2):185-8. PubMed ID: 2737915 [No Abstract] [Full Text] [Related]
19. Study of abnormal hemoglobin in Ehime, Japan: two structural variants of hemoglobin A (Hb I and Hb J Iran) and structural and synthetic variants of delta chain. Saito S Jinrui Idengaku Zasshi; 1984 Sep; 29(3):335-51. PubMed ID: 6085353 [No Abstract] [Full Text] [Related]