Literature DB >> 14219426

RELATIONSHIP OF HEMOGLOBIN BART'S AND H TO ALPHA THALASSEMIA.

D J WEATHERALL.   

Abstract

Entities:  

Keywords:  GENETICS, HUMAN; HEMOGLOBIN C; HEMOGLOBINS, ABNORMAL; INFANT; INFANT, NEWBORN; MARYLAND; NEGROES; THALASSEMIA

Mesh：

Substances：

Year:  1964        PMID： 14219426     DOI： 10.1111/j.1749-6632.1965.tb54047.x

Source DB:  PubMed          Journal:  Ann N Y Acad Sci        ISSN： 0077-8923            Impact factor:   5.691


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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.  Thalassaemia.

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

3.  [Alpha-thalassemia with HbH and Hb Bart's in a German family].

Authors:  P Rönisch; E Kleihauer
Journal:  Klin Wochenschr       Date:  1967-12-01

4.  Differences between alpha- and beta-chain mutants of human haemoglobin and between alpha- and beta-thalassaemia. Possible duplication of the alpha-chain gene.

Authors:  H Lehmann; R W Carrell
Journal:  Br Med J       Date:  1968-12-21

5.  Is the doubly deleted alpha-thalassemia gene a "fugitive" allele?

Authors:  C Wills; D R Londo
Journal:  Am J Hum Genet       Date:  1981-03       Impact factor: 11.025

6.  EF Bart's Disease with Coinheritance of Gγ-XmnI and Aγ-Globin Polymorphisms: A Case of Nontransfusion-Dependant Thalassemia.

Authors:  Kane M Laks; Cara Hirner; Barbara Gruner; Jared Coberly; Katsiaryna Laziuk; Bindu Kanathezhath Sathi
Journal:  Case Rep Hematol       Date:  2020-10-30
  6 in total

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