Literature DB >> 13908956

A family with S and C hemoglobins and the hereditary persistence of F hemoglobin. A comparison of C thalassemia disease with the CF syndrome.

R G SCHNEIDER, W C LEVIN, C EVERETT.   

Abstract

Entities:  

Keywords:  ANEMIA, ERYTHROBLASTIC/genetics; ANEMIA, SICKLE CELL/genetics; HEMOGLOBIN/abnormalities

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Year:  1961        PMID： 13908956     DOI： 10.1056/NEJM196112282652602

Source DB:  PubMed          Journal:  N Engl J Med        ISSN： 0028-4793            Impact factor:   91.245


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  3 in total

1.  Combinations of high levels of hemoglobin F with haemoglobins A, S, and C in Ghana.

Authors:  G R THOMPSON; H LEHMANN
Journal:  Br Med J       Date:  1962-06-02

2.  Balanced globin chain synthesis in hereditary persistence of fetal hemoglobin.

Authors:  C L Natta; G A Niazi; S Ford; A Bank
Journal:  J Clin Invest       Date:  1974-08       Impact factor: 14.808

3.  Hereditary persistence of fetal hemoglobin, beta thalassemia, and the hemoglobin delta-beta locus: further family data and genetic interpretations.

Authors:  N C Bethlenfalvay; A G Motulsky; B Ringelhann; H Lehmann; J R Humbert; F I Konotey-Ahulu
Journal:  Am J Hum Genet       Date:  1975-03       Impact factor: 11.025
  3 in total

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