Literature DB >> 14197371

HAEMOGLOBIN GACCA.

F S BOI-DOKU, H LEHMANN, D BEALE.   

Abstract

Keywords:  AMINO ACIDS; AUTOANALYSIS; CHEMISTRY, ANALYTICAL; CHROMATOGRAPHY; ELECTROPHORESIS; HEMOGLOBIN; PEPTIDES

Mesh：

Substances：

Year:  1964        PMID： 14197371     DOI： 10.1038/203363a0

Source DB:  PubMed          Journal:  Nature        ISSN： 0028-0836            Impact factor:   49.962


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  11 in total

1.  Homozygous haemoglobin D Punjab.

Authors:  C Politis-Tsegos; P Kynoch; A Lang; H Lehmann; P A Lorkin; R Stathopoulou; G Wakefield
Journal:  J Med Genet       Date:  1975-09       Impact factor: 6.318

Review 2.  HUMAN HAEMOGLOBINS.

Authors:  E R HUEHNS; E M SHOOTER
Journal:  J Med Genet       Date:  1965-03       Impact factor: 6.318

Review 3.  Haemoglobin D Punjab (D Los Angeles).

Authors:  F Vella; H Lehmann
Journal:  J Med Genet       Date:  1974-12       Impact factor: 6.318

4.  Are human hemoglobin variants distributed randomly among the positions?

Authors:  W M Fitch
Journal:  J Mol Evol       Date:  1973       Impact factor: 2.395

Review 5.  Molecular basis of hereditary disease.

Authors:  H Harris
Journal:  Br Med J       Date:  1968-04-20

6.  Haemoglobin Korle-Bu (beta 73 aspartic acid replaced by asparagine) showing one of the two amino acid substitutions of haemoglobin C Harlem.

Authors:  F I Konotey-Ahulu; E Gallo; H Lehmann; B Ringelhann
Journal:  J Med Genet       Date:  1968-06       Impact factor: 6.318

7.  High incidence of haemoglobin G Accra in a rural district in Jamaica.

Authors:  P F Milner
Journal:  J Med Genet       Date:  1967-06       Impact factor: 6.318

8.  [Hemoglobin Köln disease: familial hypochromic hemolytic anemia with hemoglobin anomaly].

Authors:  W Pribilla; P Klesse; K Betke; H Lehmann; D Beale
Journal:  Klin Wochenschr       Date:  1965-10-01

9.  Hemoglobin Hasharon (alpha-2-47 his(CD5)beta-2): a hemoglobin found in low concentration.

Authors:  S Charache; A M Mondzac; U Gessner
Journal:  J Clin Invest       Date:  1969-05       Impact factor: 14.808

10.  Sickle-cell anaemia, sickle-cell thalassaemia, sickle-cell haemoglobin C disease, and asymptomatic haemoglobin C thalassaemia in one Ghanaian family.

Authors:  F I Konotey-Ahulu; B Ringelhann
Journal:  Br Med J       Date:  1969-03-08
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