Literature DB >> 13723916

Haemoglobin Q-alpha-thalassaemia.

K M DORMANDY, S P LOCK, H LEHMANN.   

Abstract

Keywords:  ANEMIA, ERYTHROBLASTIC/case reports; HEMOGLOBIN

Mesh:

Substances:

Year:  1961        PMID: 13723916      PMCID: PMC1954197          DOI: 10.1136/bmj.1.5239.1582

Source DB:  PubMed          Journal:  Br Med J        ISSN: 0007-1447


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  12 in total

1.  Genetic basis of the thalassaemia diseases.

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

2.  Identity of haemoglobin A2.

Authors:  C J MULLER; J H JONXIS
Journal:  Nature       Date:  1960-12-10       Impact factor: 49.962

3.  Identity of the alpha-chains of adult and foetal human haemoglobins.

Authors:  J A HUNT
Journal:  Nature       Date:  1959-05-16       Impact factor: 49.962

4.  Hemoglobin H associated with an uncommon variant of thalassemia trait.

Authors:  W A DITTMAN; A HAUT; M M WINTROBE; G E CARTWRIGHT
Journal:  Blood       Date:  1960-07       Impact factor: 22.113

5.  The electrophoretic characterization of haemoglobin G and a new minor haemoglobin. G2.

Authors:  E M SHOOTER; E R SKINNER; J P GARLICK; N A BARNICOT
Journal:  Br J Haematol       Date:  1960-04       Impact factor: 6.998

6.  [On a protein accompanying hemoglobin of adult man and its concentration in isolated fractions of alkaline-resistant hemoglobin].

Authors:  Y DERRIEN; G LAURENT; M BORGOMANO
Journal:  C R Hebd Seances Acad Sci       Date:  1956-03-12

7.  Observations on some fast haemoglobins: K, J, N, and Bart's.

Authors:  J A AGER; H LEHMANN
Journal:  Br Med J       Date:  1958-04-19

8.  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

9.  Starch gel electrophoresis in a discontinous system of buffers.

Authors:  M D POULIK
Journal:  Nature       Date:  1957-12-28       Impact factor: 49.962

10.  Studies on abnormal hemoglobins. I. Their demonstration in sickle cell anemia and other hematologic disorders by means of alkali denaturation.

Authors:  K SINGER; A I CHERNOFF; L SINGER
Journal:  Blood       Date:  1951-05       Impact factor: 22.113

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  12 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.  THALASSAEMIA IN SCOTS.

Authors:  K D BUCHANAN; J D KINLOCH; H E HUTCHISON; P H PINKERTON; P CASSIDY
Journal:  J Clin Pathol       Date:  1963-11       Impact factor: 3.411

3.  BETA THALASSEMIA-HEMOGLOBIN D ALPHA. A FAMILY REPORT.

Authors:  R C LEE; T H HUISMAN
Journal:  Am J Hum Genet       Date:  1965-03       Impact factor: 11.025

Review 4.  HUMAN HAEMOGLOBINS.

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

5.  [Hemoglobin anomalies].

Authors:  K BETKE
Journal:  Blut       Date:  1961

6.  Thalassaemia.

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

7.  An unusual hemoglobin anomaly and its relation to alpha-thalassemia and hemoglobin-H disease.

Authors:  G D Efremov; R N Wrightstone; T H Huisman; W A Schroeder; C Hyman; J Ortega; K Williams
Journal:  J Clin Invest       Date:  1971-08       Impact factor: 14.808

8.  Thalassemia genes.

Authors:  P Wasi
Journal:  Br Med J       Date:  1970-02-14

9.  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

10.  Globin chain synthesis in the alpha thalassemia syndromes.

Authors:  Y W Kan; E Schwartz; D G Nathan
Journal:  J Clin Invest       Date:  1969-11       Impact factor: 14.808

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