Literature DB >> 14478740

Homozygous Lepore haemoglobin disease appearing as thalassaemia major in two Papuan siblings.

H NEEB, J L BEIBOER, J H JONXIS, J A KAARS SIJPESTEIJN, C J MULLER.   

Abstract

Keywords:  ANEMIA, ERYTHROBLASTIC/in infancy and childhood; HEMOGLOBIN/abnormalities

Mesh：

Substances：

Year:  1961        PMID： 14478740

Source DB:  PubMed          Journal:  Trop Geogr Med        ISSN： 0041-3232


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  5 in total

1.  The fusion of two peptide chains in hemoglobin Lepore and its interpretation as a genetic deletion.

Authors:  C BAGLIONI
Journal:  Proc Natl Acad Sci U S A       Date:  1962-11-15       Impact factor: 11.205

2.  [Hemoglobin anomalies].

Authors:  K BETKE
Journal:  Blut       Date:  1961

3.  Thalassaemia.

Authors:  E R Huehns
Journal:  Postgrad Med J       Date:  1965-12       Impact factor: 2.401

4.  [Hb Frankfurt: a new unstable haemoglobin. II. Attempts to elucidate the structural aberrations].

Authors:  L Nowicki; H Martin
Journal:  Klin Wochenschr       Date:  1972-05-01

5.  Gene duplication as the basis for amino acid ambiguity in the alpha-chain polypeptides of mouse hemoglobins.

Authors:  K Hilse; R A Popp
Journal:  Proc Natl Acad Sci U S A       Date:  1968-11       Impact factor: 11.205
  5 in total

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