| 1 | HPFH, HBG1, PRPF19, GTF2F1
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| Purification and identification of proteins that bind to the hereditary persistence of fetal hemoglobin -198 mutation in the gamma-globin gene promoter.
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| Olave IA, Doneanu C, Fang X, Stamatoyannopoulos G, Li Q.
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| J Biol Chem 282(2):853-62. Epub 2006 Nov 17. 2007
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| 2 | HPFH, LCR-HB-B@, TGDB
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| Deletion of a region that is a candidate for the difference between the deletion forms of hereditary persistence of fetal hemoglobin and delta beta-thalassemia affects beta- but not gamma-globin gene expression.
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| Calzolari R, et al.
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| EMBO J 18 : 949-958. 1999
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| 3 | HBG1, HPFH
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| The Cretan type of non-deletional hereditary persistence of fetal hemoglobin [Agamma-158C-T] results from two independent gene conversion events.
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| Patrinos GP, et al.
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| Hum Genet 102 : 629-634. 1998
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| 4 | HPFH, OR51A10P
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| Molecular cloning of the breakpoints of the hereditary persistence of fetal hemoglobin type-6 (HPFH-6) deletion and sequence analysis of the novel juxtaposed region from the 3' end of the beta-globin gene cluster.
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| Kosteas T, Palena A, Anagnou NP.
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| Hum Genet 100(3-4):441-5. 1997
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| 5 | HPFH
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| Molecular identification of hereditary persistence of fetal hemoglobin type 2 (HPFH type 2) in patients from Brazil.
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| Gon¨alves MS, et al.
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| Ann Hematol 70 : 159-161. 1995
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| 6 | HPFH
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| Nondeletional type of hereditary persistence of fetal haemoglobin : molecular characterization of three unrelated Thai HPFH.
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| Winichagoon P, et al.
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| Br J Haematol 87 : 797-804. 1994
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| 7 | HPFH, HPFH3, FCP1
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| Detection of a major gene for heterocellular hereditary persistence of fetal hemoglobin after accounting for genetic modifiers.
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| Thein SL, et al.
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| Am J Hum Genet 54 : 214-228. 1994
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| 8 | HPFH
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| Molecular characterisation of Vietnamese HPFH.
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| Motum PI, et al.
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| Hum Mutat 2 : 179-184. 1993
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| 9 | HPFH
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| A single point mutation is the cause of the Greek form of hereditary persistence of fetal haemoglobin.
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| Berry M, et al.
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| Nature 358 : 499-502. 1992
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| 10 | HPFH, HBG1
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| Rapid identification by denaturing gradient gel electrophoresis of mutations in the gamma-globin gene promoters in non-deletion type HPFH.
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| Gottardi E, et al.
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| Br J Haematol 80 : 533-538. 1992
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| 11 | HPFH, HBG1
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| The Georgia type of nondeletial hereditary persistence of fetal hemoglobin has a C-T mutation at nucleotide -114 of the Agamma-globin gene.
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| …ner R, et al.
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| Blood 77 : 1124-1128. 1991
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| 12 | HPFH
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| Translocation of an erythroid-specific hypersensitive site in deletion-type hereditary persistence of fetal hemoglobin.
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| Elder JT, et al.
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| Mol Cell Biol 10 : 1382-1389. 1990
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| 13 | HPFH
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| A new hereditary persistence of fetal hemoglobin deletion has the breakpoint within the 3' beta-globin gene enhancer.
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| Camaschella C, et al.
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| Blood 75 : 1000-1005. 1990
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| 14 | HPFH, HBG1
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| Molecular diagnosis of Agamma hereditary persistence of fetal hemoglobin using polymerase chain reaction and oligonucleotide analysis.
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| Gottardi E, et al.
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| Haematologica 75 : 17-20. 1990
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| 15 | HPFH
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| The Brazilian type of nondeletional A-gamma-fetal hemoglobin has A C-G substitution at nucleotide -195 of the A-gamma-globin gene.
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| Costa FF, et al.
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| Blood 76 : 1896-1897. 1990
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| 16 | HPFH
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| A case of hereditary persistence of fetal hemoglobin caused by a gene not linked to the beta-globin cluster.
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| Martinez G, et al.
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| Hum Genet 82 : 335-337. 1989
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| 17 | FCP1, HPFH
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| Hemoglobin F production in heterocellular hereditary persistence of fetal hemoglobin and its linkage to the beta globin gene complex.
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| Donald JA, Lammi A, Trent RJ.
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| Hum Genet 80(1):69-74. 1988
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| 18 | HPFH, HBB
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| Identification of base substitutions in the promoter regions of the Agamma- and Ggamma-globin genes in Agamma-(or Ggamma-)beta+-HPFH heterozygotes using the DNA-amplification-synthetic oligonucleotide procedure.
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| Yang KG, et al.
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| Blood 71 : 1414-1417. 1988
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| 19 | HPFH
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| The deletion in both common types of hereditary persistence of fetal hemoglobin is approximately 105 kilobases.
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| Collins FS, et al.
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| Blood 70 : 1797-1803. 1987
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| 20 | HPFH
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| Developmental regulation of human globin genes.
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| Karlsson S, et al.
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| Annu Rev Biochem 54 : 1071-1108. 1985
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| 21 | HPFH
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| The -158 site 5' to the G-gamma gene and G-gamma expression.
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| Labie D, et al.
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| Blood 66 : 1463-1465. 1985
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| 22 | HPFH
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| DNA sequence variation associated with elevated fetal G-gamma globin production.
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| Gilman JG, et al.
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| Blood 66 : 783-787. 1985
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| 23 | HPFH
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| Heterocellular hereditary persistence of fetal hemoglobin (HPFH). Molecular mechanisms of abnormal gamma-gene expression in association with beta-thalassemia and linkage relationship with the beta-globin gene cluster.
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| Giampaolo A, et al.
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| Hum Genet 66 : 151-156. 1984
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| 24 | HPFH
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| Molecular comparison of delta beta-thalassemia and hereditary persistence of fetal hemoglobin DNAs : evidence of a regulatory area?
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| Ottolenghi S, et al.
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| Proc Natl Acad Sci U S A 79 : 2347-2351. 1982
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| 25 | HPFH
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| Genetic regulation of gamma gene expression : study of the interaction of beta-thalassemia with heterocellular HPFH.
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| Soummer AM, et al.
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| Hum Genet 57 : 371-375. 1981
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