Literature DB >> 889715

Heterocellular hereditary persistence of fetal haemoglobin (heterocellular HPFH) and its interaction with beta thalassaemia.

W G Wood, D J Weatherall, J B Clegg, T J Hamblin, J H Edwards, A M Barlow.   

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Year:  1977        PMID： 889715     DOI： 10.1111/j.1365-2141.1977.tb00986.x

Source DB:  PubMed          Journal:  Br J Haematol        ISSN： 0007-1048            Impact factor:   6.998


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  11 in total

1.  Detection of non-deletional type of hereditary persistence of fetal hemoglobin (HPFH) condition associated with 619 bp β(°)-thalassemia deletion.

Authors:  S M Husain; M P Anandaraj
Journal:  Indian J Clin Biochem       Date:  1997-07

2.  Hemoglobin F production in heterocellular hereditary persistence of fetal hemoglobin and its linkage to the beta globin gene complex.

Authors:  J A Donald; A Lammi; R J Trent
Journal:  Hum Genet       Date:  1988-09       Impact factor: 4.132

3.  DNA methylation in hereditary persistence of fetal hemoglobin (HPFH-2).

Authors:  M Poncz; M Sutton; K Delgrosso; E Schwartz; S Surrey
Journal:  Nucleic Acids Res       Date:  1987-07-10       Impact factor: 16.971

4.  Sickle beta 0 thalassemia in Eastern Saudi Arabia.

Authors:  M E Pembrey; R P Perrine; W G Wood; D J Weatherall
Journal:  Am J Hum Genet       Date:  1980-01       Impact factor: 11.025

5.  Clinical and haematological evaluation of beta thalassaemia intermedia with increased Hb F and Hb A2 in heterozygotes: beta thalassaemia intermedia I.

Authors:  C Altay; A Gurgey
Journal:  J Med Genet       Date:  1985-06       Impact factor: 6.318

6.  G gamma beta+ hereditary persistence of fetal hemoglobin: cosmid cloning and identification of a specific mutation 5' to the G gamma gene.

Authors:  F S Collins; C J Stoeckert; G R Serjeant; B G Forget; S M Weissman
Journal:  Proc Natl Acad Sci U S A       Date:  1984-08       Impact factor: 11.205

7.  Heterogeneity of sickle-cell anemia based on a profile of hematological variables.

Authors:  D J Odenheimer; C F Whitten; D L Rucknagel; S A Sarnaik; C F Sing
Journal:  Am J Hum Genet       Date:  1983-11       Impact factor: 11.025

Review 8.  The thalassemias: molecular mechanisms of human genetic disease.

Authors:  R A Spritz; B G Forget
Journal:  Am J Hum Genet       Date:  1983-05       Impact factor: 11.025

9.  Fetal haemoglobin, sickling, and thalassaemia: a therapeutic lead?

Authors: 
Journal:  Br Med J       Date:  1978-07-01

10.  Genetic regulation of gamma gene expression: study of the interaction of beta-thalassemia with heterocellular HPFH.

Authors:  A M Soummer; U Testa; P Dujardin; A Guerrasio; A Henri; M Gazaix; J Riou; H Rochant; Y Beuzard; J Rosa
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132
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