Literature DB >> 14484764

Erythrokinetics in thalassemia. II. Studies in Lepore trait and hemoglobin H disease.

H A PEARSON, W McFARLAND.   

Abstract

Entities:  

Keywords:  ANEMIA, ERYTHROBLASTIC/blood; HEMOGLOBIN

Mesh：

Substances：

Year:  1962        PMID： 14484764

Source DB:  PubMed          Journal:  J Lab Clin Med        ISSN： 0022-2143


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  4 in total

1.  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

2.  [HEMOGLOBIN H IN TURKEY].

Authors:  V GOEKSEL; M A BOELUEKOGLU; N AKPINAR; M ASLAN; N TARTAROGLU
Journal:  Blut       Date:  1964-09

3.  Haemoglobin LeporeBoston in a Turkish family.

Authors:  A O Cavdar; A Arcasoy
Journal:  J Med Genet       Date:  1976-10       Impact factor: 6.318

4.  [Hb Frankfurt: a new unstable haemoglobin. II. Attempts to elucidate the structural aberrations].

Authors:  L Nowicki; H Martin
Journal:  Klin Wochenschr       Date:  1972-05-01
  4 in total

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