Literature DB >> 14205978

INTERACTION OF BETA-THALASSAEMIA AND HEREDITARY PERSISTENCE OF FOETAL HAEMOGLOBIN.

G W BIRD, M I HASAN, O P MALHOTRA, H LEHMANN.   

Abstract

Keywords:  CHILD; DIAGNOSIS; ETHNOLOGY; FETAL HEMOGLOBIN; GENETICS, HUMAN; HEMOGLOBINS, ABNORMAL; THALASSEMIA

Mesh：

Substances：

Year:  1964        PMID： 14205978      PMCID： PMC1012719          DOI： 10.1136/jmg.1.1.24

Source DB:  PubMed          Journal:  J Med Genet        ISSN： 0022-2593            Impact factor:   6.318


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  5 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.  Observations on the high foetal haemoglobin gene and its interaction with the thalassaemia gene.

Authors:  P BARKHAN; M ADINOLFI
Journal:  J Clin Pathol       Date:  1962-07       Impact factor: 3.411

3.  Folic-acid deficiency in thalassaemia major.

Authors:  A L LUHBY; J M COOPERMAN
Journal:  Lancet       Date:  1961-08-26       Impact factor: 79.321

4.  Two families showing interaction of haemoglobin C or thalassaemia with high foetal haemoglobin in adults.

Authors:  A P KRAUS; B KOCH; L BURCKETT
Journal:  Br Med J       Date:  1961-05-20

5.  The hemoglobin genes: a remarkable example of the clustering of related genetic functions on a single mammalian chromosome.

Authors:  J V NEEL
Journal:  Blood       Date:  1961-12       Impact factor: 22.113
  5 in total
  1 in total

Review 1.  Haemoglobinopathies, glucose-6-phosphate dehydrogenase deficiency and allied problems in the Indian subcontinent.

Authors:  J B Chatterjea
Journal:  Bull World Health Organ       Date:  1966       Impact factor: 9.408
  1 in total

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