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April 1, 1994American Journal of Hematology

Two different mutations in codon 68 are observed in Hb G‐Philadelphia heterozygotes

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Authors

TMT. P. MolchanovaLomonosov Moscow State UniversityDPD. D. PobedimskayaInternational Science and Technology CenterZYZ. YeAugusta University

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Cite This Study

Molchanova et al. (1994) studied this question.

synapsesocial.com/papers/6a98e881ea739e5cccf5a1e5https://doi.org/10.1002/ajh.2830450414
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Also Consider

Synapse has enriched 3 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Construction of Human Gene Libraries from Small Amounts cf Peripheral Blood: Analysis of β-Like Globin Genes1982 · 568 citations
  2. 2Studies on the Proportion and Synthesis of Haemoglobin G Philadelphia in Red Cells of Heterozygotes, a Homozygote, and a Heterozygote for both Haemoglobin G and α Thalassaemia1976 · 55 citations
  3. 3Alternate Organization of α G-Philadelphia Globin Genes Among U.S. Black and Italian Caucasian Heterozygotes1984 · 14 citations