95 related articles for article (PubMed ID: 2445255)
1. [Analysis of the recombination zone in hereditary persistence of fetal hemoglobin with fetal gene rearrangement of the G gamma-G gamma-A gamma type].
Vidaud-Raphanaud D; Bouhassira E; Labie D; Krishnamoorthy R
Ann Genet; 1987; 30(3):133-7. PubMed ID: 2445255
[TBL] [Abstract][Full Text] [Related]
2. Differential diagnosis of adult hemoglobin A, F, and S conditions. A case of G gamma-beta(+)-hereditary persistence of fetal hemoglobin.
Carter DK; Lucia MS; Winter SD
Arch Pathol Lab Med; 1991 May; 115(5):533-6. PubMed ID: 1708658
[TBL] [Abstract][Full Text] [Related]
3. Delta beta thalassemia and hereditary persistence of fetal hemoglobin.
Bollekens JA; Forget BG
Hematol Oncol Clin North Am; 1991 Jun; 5(3):399-422. PubMed ID: 1713909
[TBL] [Abstract][Full Text] [Related]
4. [Hereditary persistence of fetal hemoglobin associated with mutation above the gamma gene].
Vidaud-Raphanaud D; Badoual J; Labie D
Arch Fr Pediatr; 1988 May; 45(5):315-7. PubMed ID: 2458081
[TBL] [Abstract][Full Text] [Related]
5. Molecular and hematological characterization of HPFH-6/Indian deletion-inversion Ggamma(Agammadeltabeta)0-thalassemia and Ggamma(Agammadeltabeta)0-thalassemia/HbE in Thai patients.
Fucharoen S; Pengjam Y; Surapot S; Fucharoen G; Sanchaisuriya K
Am J Hematol; 2002 Oct; 71(2):109-13. PubMed ID: 12353310
[TBL] [Abstract][Full Text] [Related]
6. G gamma-196 C-->T, A gamma-201 C-->T: two novel mutations in the promoter region of the gamma-globin genes associated with nondeletional hereditary persistence of fetal hemoglobin in Greece.
Tasiopoulou M; Boussiou M; Sinopoulou K; Moraitis G; Loutradi-Anagnostou A; Karababa P
Blood Cells Mol Dis; 2008; 40(3):320-2. PubMed ID: 18096417
[TBL] [Abstract][Full Text] [Related]
7. Molecular characterization of delta beta-thalassemia and hereditary persistence of fetal hemoglobin in the Indian population.
Nadkarni A; Wadia M; Gorakshakar A; Kiyama R; Colah RB; Mohanty D
Hemoglobin; 2008; 32(5):425-33. PubMed ID: 18932066
[TBL] [Abstract][Full Text] [Related]
8. Dissecting the loci controlling fetal haemoglobin production on chromosomes 11p and 6q by the regressive approach.
Craig JE; Rochette J; Fisher CA; Weatherall DJ; Marc S; Lathrop GM; Demenais F; Thein S
Nat Genet; 1996 Jan; 12(1):58-64. PubMed ID: 8528252
[TBL] [Abstract][Full Text] [Related]
9. Disorders of the synthesis of human fetal hemoglobin.
Manca L; Masala B
IUBMB Life; 2008 Feb; 60(2):94-111. PubMed ID: 18379999
[TBL] [Abstract][Full Text] [Related]
10. Unusual combination of genetic defects in a Sicilian boy: G gamma delta beta thalassemia, G gamma A gamma heterocellular HPFH, beta (0) thalassemia, and albinism.
Schilirò G; Pavone L; Romeo MA; Russo A; Musumeci S; Russo G
Am J Med Genet; 1983 Jun; 15(2):225-31. PubMed ID: 6192718
[TBL] [Abstract][Full Text] [Related]
11. Hemoglobin Kenya composed of alpha- and ((A)gammabeta)-fusion-globin chains, associated with hereditary persistence of fetal hemoglobin.
Wilcox I; Boettger K; Greene L; Malek A; Davis L; Steinberg MH; Luo HY; Chui DH
Am J Hematol; 2009 Jan; 84(1):55-8. PubMed ID: 19006227
[TBL] [Abstract][Full Text] [Related]
12. 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 newborn.
Huisman TH; Efremov GD; Reese AL; Howard JS; Gravely ME; Harris HF; Wilson JB
Hemoglobin; 1979; 3(4):223-52. PubMed ID: 500369
[TBL] [Abstract][Full Text] [Related]
13. A non-deletion hereditary persistence of fetal hemoglobin (HPFH) determinant not linked to the beta-globin gene complex.
Thein SL; Weatherall DJ
Prog Clin Biol Res; 1989; 316B():97-111. PubMed ID: 2482508
[TBL] [Abstract][Full Text] [Related]
14. A new type of hereditary persistence of fetal haemoglobin (HPFH): HPFH Tunisia beta + (+C-200)G gamma.
Pissard S; M'rad A; Beuzard Y; Roméo PH
Br J Haematol; 1996 Oct; 95(1):67-72. PubMed ID: 8857940
[TBL] [Abstract][Full Text] [Related]
15. Compound heterozygote state for GgammaAgamma(deltabeta) degrees -thalassemia and hereditary persistence of fetal hemoglobin.
Fucharoen S; Panyasai S; Surapot S; Fucharoen G; Sanchaisuriya K
Am J Hematol; 2005 Oct; 80(2):119-23. PubMed ID: 16184575
[TBL] [Abstract][Full Text] [Related]
16. Molecular basis and hematologic characterization of deltabeta-thalassemia and hereditary persistence of fetal hemoglobin in Thailand.
Panyasai S; Fucharoen S; Surapot S; Fucharoen G; Sanchaisuriya K
Haematologica; 2004 Jul; 89(7):777-81. PubMed ID: 15257928
[TBL] [Abstract][Full Text] [Related]
17. Restriction endonuclease gene mapping studies of an Indian (A gamma delta beta)zero-thalassaemia, previously identified as G gamma-HPFH.
Nakatsuji T; Gilman JG; Sukumaran PK; Huisman TH
Br J Haematol; 1984 Aug; 57(4):663-70. PubMed ID: 6204682
[TBL] [Abstract][Full Text] [Related]
18. Screening of Iranian thalassemic families for the most common deletions of the beta-globin gene cluster.
Esteghamat F; Imanian H; Azarkeivan A; Pourfarzad F; Almadani N; Najmabadi H
Hemoglobin; 2007; 31(4):463-9. PubMed ID: 17994380
[TBL] [Abstract][Full Text] [Related]
19. Globin gene expression in hereditary persistence of fetal haemoglobin and (delta beta) (0)-thalassaemia.
Poncz M; Henthorn P; Stoeckert C; Surrey S
Oxf Surv Eukaryot Genes; 1988; 5():163-203. PubMed ID: 2472152
[TBL] [Abstract][Full Text] [Related]
20. [The molecular basis of hereditary persistence of fetal hemoglobin (HPFH). Clinical importance of the hemoglobin switching mechanism with special reference to Corfu delta beta zero thalassemia].
Kulozik AE; Kohne E; Kleihauer E
Monatsschr Kinderheilkd; 1988 Nov; 136(11):751-7. PubMed ID: 2464759
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]