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December 1, 1984BloodOpen Access

Concordance of a point mutation 5' to the G gamma globin gene with G gamma beta +. Hereditary persistence of fetal hemoglobin in the black population

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Authors

FCFS CollinsNational Institutes of HealthCBCD BoehmThe University of SydneyPWPG WaberThe University of Texas Southwestern Medical Center

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Cite This Study

Collins et al. (1984) studied this question.

synapsesocial.com/papers/69daa40fa6045d71bfa3d5f3https://doi.org/10.1182/blood.v64.6.1292.1292
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Also Consider

Synapse has enriched 4 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1G gamma beta+ hereditary persistence of fetal hemoglobin: cosmid cloning and identification of a specific mutation 5' to the G gamma gene.1984 · 140 citations
  2. 2Heterocellular Hereditary Persistence of Fetal Haemoglobin (Heterocellular HPFH) and its Interaction with β Thalassaemia1977 · 49 citations
  3. 3Physical mapping of the globin gene deletion in hereditary persistence of foetal haemoglobin (HPFH)1980 · 154 citations
  4. 4Insertion of synthetic copies of human globin genes into bacterial plasmids1978 · 348 citations