Literature DB >> 13929130

Study of a family possessing hemoglobin C, classical thalassemia and the abnormal minor hemoglobin component A2.

R C LEE, T H HUISMAN.   

Abstract

Entities:  

Keywords:  ANEMIA, ERYTHROBLASTIC; HEMOGLOBIN C; HEMOGLOBINS, ABNORMAL

Mesh：

Substances：

Year:  1963        PMID： 13929130      PMCID： PMC1932438     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN： 0002-9297            Impact factor:   11.025


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  6 in total

1.  Genetic basis of the thalassaemia diseases.

Authors:  V M INGRAM; A O STRETTON
Journal:  Nature       Date:  1959-12-19       Impact factor: 49.962

2.  Properties and inheritance of the new fast hemoglobin type found in umbilical cord blood samples of Negro babies.

Authors:  T H HUISMAN
Journal:  Clin Chim Acta       Date:  1960-09       Impact factor: 3.786

3.  Studies on an abnormal minor hemoglobin component (Hb-B2).

Authors:  B HORTON; R A PAYNE; M T BRIDGES; T H HUISMAN
Journal:  Clin Chim Acta       Date:  1961-03       Impact factor: 3.786

4.  Thalassemia minor associated with hemoglobin-B2 heterozygosity. A family report.

Authors:  T H HUISMAN; K PUNT; J D SCHAAD
Journal:  Blood       Date:  1961-06       Impact factor: 22.113

5.  Allelomorphism and the chemical differences of the human haemoglobins A, S and C.

Authors:  J A HUNT; V M INGRAM
Journal:  Nature       Date:  1958-04-12       Impact factor: 49.962

6.  Determination of low percentages of fetal hemoglobin in blood of normal children.

Authors:  J H JONXIS; H K VISSER
Journal:  AMA J Dis Child       Date:  1956-12
  6 in total

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