Literature DB >> 13208756

Thalassemia-hemoglobin C disease; a new syndrome presumably due to the combination of the genes for thalassemia and hemoglobin C.

W W ZUELZER, E KAPLAN.   

Abstract

Entities:  

Keywords:  ANEMIA, ERYTHROBLASTIC/blood in; HEMOGLOBIN/abnormalities

Mesh:

Substances:

Year:  1954        PMID: 13208756

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


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  8 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

Review 2.  HUMAN HAEMOGLOBINS.

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

3.  [Types of human hemoglobin; physiological and pathological significance].

Authors:  A C ALLISON
Journal:  Klin Wochenschr       Date:  1958-05-01

4.  The abnormal hemoglobins.

Authors:  A B HENDERSON
Journal:  J Natl Med Assoc       Date:  1956-07       Impact factor: 1.798

5.  [Abnormal human hemoglobin].

Authors:  K BETKE
Journal:  Klin Wochenschr       Date:  1956-02-01

6.  Thalassaemia.

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

7.  [Hemoglobin C in Europeans: 1 new, probable homozygote and 3 heterozygote carriers of the anomaly].

Authors:  H R Marti; H Lehmann; G Keiser; W Siegenthaler
Journal:  Blut       Date:  1965-09

8.  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
  8 in total

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