Literature DB >> 4793127

A second type of hereditary persistence of foetal haemoglobin in India.

W A Schroeder, T H Huisman, P K Sukumaran.   

Abstract

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Year:  1973        PMID： 4793127     DOI： 10.1111/j.1365-2141.1973.tb01722.x

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


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  5 in total

1.  Translocation of an erythroid-specific hypersensitive site in deletion-type hereditary persistence of fetal hemoglobin.

Authors:  J T Elder; W C Forrester; C Thompson; D Mager; P Henthorn; M Peretz; T Papayannopoulou; M Groudine
Journal:  Mol Cell Biol       Date:  1990-04       Impact factor: 4.272

2.  A gene deletion ending within a complex array of repeated sequences 3' to the human beta-globin gene cluster.

Authors:  P S Henthorn; D L Mager; T H Huisman; O Smithies
Journal:  Proc Natl Acad Sci U S A       Date:  1986-07       Impact factor: 11.205

Review 3.  Manipulation of Developmental Gamma-Globin Gene Expression: an Approach for Healing Hemoglobinopathies.

Authors:  Vigneshwaran Venkatesan; Saranya Srinivasan; Prathibha Babu; Saravanabhavan Thangavel
Journal:  Mol Cell Biol       Date:  2020-12-21       Impact factor: 4.272

4.  Heterogeneity in the molecular basis of three types of hereditary persistence of fetal hemoglobin and the relative synthesis of the G gamma and A gamma types of gamma chain.

Authors:  A Kutlar; M B Gardiner; M G Headlee; A L Reese; M P Cleek; S Nagle; P K Sukumaran; T H Huisman
Journal:  Biochem Genet       Date:  1984-02       Impact factor: 1.890

5.  Thalassemia intermedia phenotype resulting from rare combination of c.46delT [Codon15 (-T)] mutation of beta globin gene and HPFH3.

Authors:  Anjali J Kelkar; Anu Moses
Journal:  Clin Case Rep       Date:  2017-05-26
  5 in total

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