These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

120 related articles for article (PubMed ID: 3718876)

  • 1. The haematological puzzle of Hb J Cape Town is partly solved.
    Lambridis AJ; Ramsay M; Jenkins T
    Br J Haematol; 1986 Jun; 63(2):363-7. PubMed ID: 3718876
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Hemoglobin constitution of double heterozygotes for alpha or beta-thalassemia and Hb J Sardegna.
    Maccioni L; Galanello R; Melis MA; Cao A
    Hemoglobin; 1984; 8(5):497-507. PubMed ID: 6548732
    [TBL] [Abstract][Full Text] [Related]  

  • 3. alpha-globin gene deletions associated with Hb J Tongariki.
    Bowden DK; Pressley L; Higgs DR; Clegg JB; Weatherall DJ
    Br J Haematol; 1982 Jun; 51(2):243-9. PubMed ID: 6979350
    [TBL] [Abstract][Full Text] [Related]  

  • 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]  

  • 20. [A first case of Hb J Paris-1 alpha2[A10] Ala----Asp beta2 carrier in Bulgaria. Structural organization].
    Molchanova TP; Zareva ZZ; Rashkov RG; Abaturov LV; Tokarev IuN
    Gematol Transfuziol; 1987 Sep; 32(9):15-9. PubMed ID: 3692118
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 6.