Literature DB >> 13662326

Multiple inherited erythrocyte abnormalities in an American Negro family: hereditary spherocytosis, sickling and thalassemia.

F COHEN, W W ZUELZER, J V NEEL, A R ROBINSON.   

Abstract

Entities:  

Keywords:  ANEMIA, ERYTHROBLASTIC; ANEMIA, SICKLE CELL; ERYTHROCYTES

Mesh：

Substances：

Year:  1959        PMID： 13662326

Source DB:  PubMed          Journal:  Blood        ISSN： 0006-4971            Impact factor:   22.113


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  6 in total

1.  Hemoglobin synthesis studies of a family with alpha-thalassemia trait and sickle cell trait.

Authors:  J R Shaeffer; J DeSimone; L J Kleve
Journal:  Biochem Genet       Date:  1975-12       Impact factor: 1.890

2.  THE COEXISTENCE OF THE GENES FOR HEMOGLOBIN E AND ALPHA-THALASSEMIA IN THAIS, WITH RESULTANT SUPPRESSION OF HEMOGLOBIN E SYNTHESIS.

Authors:  S TUCHINDA; D L RUCKNAGEL; V MINNICH; U BOONYAPRAKOB; K BALANKURA; V SUVATEE
Journal:  Am J Hum Genet       Date:  1964-09       Impact factor: 11.025

3.  The frequency of elevations in the A and fetal hemoglobin fractions in the natives of Liberia and adjacent regions, with data on haptoglobin and transferrin types.

Authors:  J V NEEL; A R ROBINSON; W W ZUELZER; F B LIVINGSTONE; H E SUTTON
Journal:  Am J Hum Genet       Date:  1961-06       Impact factor: 11.025

4.  Thalassaemia.

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

5.  Combination of spherocytosis and a variant of beta thalassaemia ('isolated raised Hb A2').

Authors:  T A Cunningham; F Vella
Journal:  J Med Genet       Date:  1967-06       Impact factor: 6.318

6.  The suppression of haemoglobin E synthesis when hemoglobin H disease and hemoglobin E trait occur together.

Authors:  S Tuchinda; D Beale; H Lehman
Journal:  Humangenetik       Date:  1967
  6 in total

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