Literature DB >> 14395263

Sickling, a quantitatively delayed genetic character.

R G SCHNEIDER, M E HAGGARD.   

Abstract

Keywords:  ANEMIA, SICKLE CELL

Mesh：

Year:  1955        PMID： 14395263     DOI： 10.3181/00379727-89-21755

Source DB:  PubMed          Journal:  Proc Soc Exp Biol Med        ISSN： 0037-9727


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  3 in total

1.  Observations on the minor basic hemoglobin component in the blood of normal individuals and patients with thalassemia.

Authors:  H G KUNKEL; R CEPPELLINI; U MULLER-EBERHARD; J WOLF
Journal:  J Clin Invest       Date:  1957-11       Impact factor: 14.808

2.  An assessment of techniques suitable for the diagnosis of sickle-cell disease and haemoglobin C disease in cord blood samples.

Authors:  G I Yaswon; R G Huntsman; J S Metters
Journal:  J Clin Pathol       Date:  1970-09       Impact factor: 3.411

3.  [Fetal and residual hemoglobin in the erythrocytes and erythroblasts of human fetuses and newborn infants].

Authors:  K BETKE; E KLEIHAUER
Journal:  Blut       Date:  1958-11
  3 in total

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