Literature DB >> 13816949

Hemoglobin H associated with an uncommon variant of thalassemia trait.

W A DITTMAN, A HAUT, M M WINTROBE, G E CARTWRIGHT.   

Abstract

Entities:  

Keywords:  ANEMIA, ERYTHROBLASTIC/case reports; HEMOGLOBIN

Mesh：

Substances：

Year:  1960        PMID： 13816949

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


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  6 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.  The abnormal haemoglobins in haemoglobin-H disease.

Authors:  N DANCE; E R HUEHNS; G H BEAVEN
Journal:  Biochem J       Date:  1963-05       Impact factor: 3.857

3.  [Hemoglobin anomalies].

Authors:  K BETKE
Journal:  Blut       Date:  1961

4.  Haemoglobin Q-alpha-thalassaemia.

Authors:  K M DORMANDY; S P LOCK; H LEHMANN
Journal:  Br Med J       Date:  1961-06-03

5.  Thalassaemia and hydrops foetalis-family studies.

Authors:  D Todd; M Lai; C A Braga
Journal:  Br Med J       Date:  1967-08-05

6.  Thalassaemia.

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

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