Literature DB >> 4846504

A new variant of sickle-cell disease with high levels of foetal haemoglobin homogeneously distributed within red cells.

M T Makler, M Berthrong, H R Locke, D L Dawson.   

Abstract

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Year:  1974        PMID： 4846504     DOI： 10.1111/j.1365-2141.1974.tb00495.x

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


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  2 in total

1.  Inheritance of F cell frequency in heterocellular hereditary persistence of fetal hemoglobin: an example of allelic exclusion.

Authors:  S H Boyer; L Margolet; M L Boyer; T H Huisman; W A Schroeder; W G Wood; D J Weatherall; J B Clegg; R Cartner
Journal:  Am J Hum Genet       Date:  1977-05       Impact factor: 11.025

2.  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
  2 in total

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