Literature DB >> 6017542

Thalassemia in Canadians.

D Dauphinee, G R Langley.   

Abstract

Thirteen Canadians with a mild hypochromic anemia were found to have beta thalassemia trait. The families of these individuals had resided in Canada for two to five generations and, where known, had not emigrated from areas with a high incidence for the thalassemia gene. A Negro family with abnormal erythrocyte morphology was suspected to be carrying the thalassemia gene although the hemoglobin A(2) concentration was normal and abnormal minor components were not detected. Thalassemia trait has been detected in practically every ethnic group, and its sporadic occurrence among Canadians without Mediterranean ancestry can be expected.

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Year:  1967        PMID: 6017542      PMCID: PMC1935952     

Source DB:  PubMed          Journal:  Can Med Assoc J        ISSN: 0008-4409            Impact factor:   8.262


  13 in total

1.  [THALASSEMIA IN QUEBEC].

Authors:  E RIOUX; J M DELAGE
Journal:  Union Med Can       Date:  1964-09

2.  THALASSAEMIA IN PEOPLE OF BRITISH STOCK.

Authors:  V A LOVRIC
Journal:  Med J Aust       Date:  1964-08-01       Impact factor: 7.738

3.  Modified apparatus for starch gel electrophoresis.

Authors:  S H BOYER; R HINER
Journal:  J Lab Clin Med       Date:  1963-05

4.  Macro and micro methods for the determination of serum iron and iron-binding capacity.

Authors:  W T CARAWAY
Journal:  Clin Chem       Date:  1963-04       Impact factor: 8.327

5.  Thalassaemia in an English and in a German family.

Authors:  F VELLA; S A IBRAHIM
Journal:  Nature       Date:  1961-08-19       Impact factor: 49.962

6.  Thalassaemia in a Scottish family.

Authors:  L G ISRAELS; H J SUDERMAN; J HOOGSTRATEN
Journal:  Lancet       Date:  1955-12-24       Impact factor: 79.321

7.  A British target-cell anaemia.

Authors:  M C ISRAELS; R L TURNER
Journal:  Lancet       Date:  1955-12-31       Impact factor: 79.321

8.  The diagnosis of thalassemia trait by starch block electrophoresis of the hemoglobin.

Authors:  P S GERALD; L K DIAMOND
Journal:  Blood       Date:  1958-01       Impact factor: 22.113

9.  Thalassaemia minor in an English-woman.

Authors:  C W HAVARD; H LEHMANN; R B SCOTT
Journal:  Br Med J       Date:  1958-02-08

10.  Studies on abnormal hemoglobins. I. Their demonstration in sickle cell anemia and other hematologic disorders by means of alkali denaturation.

Authors:  K SINGER; A I CHERNOFF; L SINGER
Journal:  Blood       Date:  1951-05       Impact factor: 22.113

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  1 in total

1.  [Thalassemia in French-speaking Quebec residents].

Authors:  L Desjardins; C Rousseau; J M Duplain; J P Valet; P Auger
Journal:  Can Med Assoc J       Date:  1978-10-07       Impact factor: 8.262

  1 in total

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