Literature DB >> 6081911

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

S Tuchinda, D Beale, H Lehman.   

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Year:  1967        PMID: 6081911     DOI: 10.1007/bf00292281

Source DB:  PubMed          Journal:  Humangenetik        ISSN: 0018-7348


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  22 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.  Sickling of erythrocytes in a patient with thalassemia-hemoglobin-I disease.

Authors:  J ATWATER; I R SCHWARTZ; A J ERSLEV; T L MONTGOMERY; L M TOCANTINS
Journal:  N Engl J Med       Date:  1960-12-15       Impact factor: 91.245

3.  Genetic basis of the thalassaemia diseases.

Authors:  V M INGRAM; A O STRETTON
Journal:  Nature       Date:  1959-12-19       Impact factor: 49.962

4.  Haemoglobin H disease with persistent haemoglobin "Bart's" in an Oriental Jewess and her daughter: a dual alpha-chain deficiency of human haemoglobin.

Authors:  B RAMOT; C SHEBA; S FISHER; J A AGER; H LEHMANN
Journal:  Br Med J       Date:  1959-12-05

5.  Properties and inheritance of haemoglobin by asymmetric recombination.

Authors:  H A ITANO; E ROBINSON
Journal:  Nature       Date:  1959-11-07       Impact factor: 49.962

6.  Sickle-cell-thalassaemia disease in South Turkey.

Authors:  M AKSOY; H LEHMANN
Journal:  Br Med J       Date:  1957-03-30

7.  A haemoglobinopathy involving haemoglobin H and a new (Q) haemoglobin.

Authors:  F VELLA; R H WELLS; J A AGER; H LEHMANN
Journal:  Br Med J       Date:  1958-03-29

8.  New hemoglobin possessing a higher electrophoretic mobility than normal adult hemoglobin.

Authors:  D A RIGAS; R D KOLER; E E OSGOOD
Journal:  Science       Date:  1955-03-11       Impact factor: 47.728

9.  Hemoglobin E, a hereditary abnormality of human hemoglobin.

Authors:  A I CHERNOFF; V MINNICH; S CHONGCHAREONSUK
Journal:  Science       Date:  1954-10-15       Impact factor: 47.728

10.  Mediterranean anemia; a study of thirty-two cases in Thailand.

Authors:  V MINNICH; S NA-NAKORN; S CHONG-CHAREONSUK; S KOCHASENI
Journal:  Blood       Date:  1954-01       Impact factor: 22.113

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  1 in total

1.  High genetic polymorphism of hemoglobin disorders in Laos. Complex phenotypes due to associated thalassemic syndromes.

Authors:  D Sicard; Y Lieurzou; C Lapoumeroulie; D Labie
Journal:  Hum Genet       Date:  1979-09       Impact factor: 4.132

  1 in total

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