Literature DB >> 2409868

Molecular analysis of deletion and nondeletion hereditary persistence of fetal hemoglobin and identification of a new mutation causing beta-thalassemia.

E A Feingold, F S Collins, J E Metherall, C J Stoeckert, S M Weissman, B G Forget.   

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Year:  1985        PMID： 2409868     DOI： 10.1111/j.1749-6632.1985.tb17185.x

Source DB:  PubMed          Journal:  Ann N Y Acad Sci        ISSN： 0077-8923            Impact factor:   5.691


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  3 in total

1.  A silent deletion in the beta-globin gene cluster.

Authors:  V E Tate; A V Hill; D K Bowden; J R Sadler; D J Weatherall; J B Clegg
Journal:  Nucleic Acids Res       Date:  1986-06-25       Impact factor: 16.971

2.  Differences between the levels of G gamma chain in the fetal hemoglobin in two types of hereditary persistence of fetal hemoglobin are linked with a variation in the DNA sequence.

Authors:  I Bakioglu; A Kutlar; T H Huisman
Journal:  Biochem Genet       Date:  1986-02       Impact factor: 1.890

3.  Molecular characterization of a novel form of (A gamma delta beta)zero-thalassemia deletion with a 3' breakpoint close to those of HPFH-3 and HPFH-4: insights for a common regulatory mechanism.

Authors:  N P Anagnou; T Papayannopoulou; A W Nienhuis; G Stamatoyannopoulos
Journal:  Nucleic Acids Res       Date:  1988-07-11       Impact factor: 16.971
  3 in total

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