Literature DB >> 13943409

A new hemoglobin variant with sickling properties.

L E PIERCE, C E RATH, K McCOY.   

Abstract

Keywords:  ANEMIA, SICKLE CELL; HEMOGLOBIN C; HEMOGLOBINS, ABNORMAL

Mesh：

Substances：

Year:  1963        PMID： 13943409     DOI： 10.1056/NEJM196304182681603

Source DB:  PubMed          Journal:  N Engl J Med        ISSN： 0028-4793            Impact factor:   91.245


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  5 in total

1.  A NEW HAEMOGLOBIN IN A THAI FAMILY. A CASE OF HAEMOGLOBIN SIRIRAJ-BETA THALASSAEMIA.

Authors:  S TUCHINDA; D BEALE; H LEHMANN
Journal:  Br Med J       Date:  1965-06-19

Review 2.  HUMAN HAEMOGLOBINS.

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

3.  Hemoglobin CHarlem (Georgetown) trait in British Columbia.

Authors:  B D Jollymore; G R Gray; S C Naiman
Journal:  CMAJ       Date:  1990-03-15       Impact factor: 8.262

4.  [Hb C homozygosity with glutathione reductase deficiency in the blood cells].

Authors:  H D Waller; J Bremer; H Schönthal; W Dorow
Journal:  Klin Wochenschr       Date:  1967-08-15

5.  Hemoglobin C trait in Saskatchewan.

Authors:  F Vella
Journal:  Can Med Assoc J       Date:  1966-11-26       Impact factor: 8.262
  5 in total

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