Literature DB >> 17948459

Genetic Study of a Family Possessing Hemoglobins S and C, and Classical Thalassemia.

P R McCurdy, H A Pearson.   

Abstract

Entities:  

Year:  1961        PMID： 17948459      PMCID： PMC1932131     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN： 0002-9297            Impact factor:   11.025


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  10 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.  Haemoglobin synthesis in thalassaemia; in-vitro studies.

Authors:  R M BANNERMAN; M GRINSTEIN; C V MOORE
Journal:  Br J Haematol       Date:  1959-01       Impact factor: 6.998

4.  Starch block electrophoresis of hemoglobin.

Authors:  H A PEARSON; W McFARLAND
Journal:  U S Armed Forces Med J       Date:  1959-06

5.  Gene mutations in human haemoglobin: the chemical difference between normal and sickle cell haemoglobin.

Authors:  V M INGRAM
Journal:  Nature       Date:  1957-08-17       Impact factor: 49.962

6.  Allelomorphism and the chemical differences of the human haemoglobins A, S and C.

Authors:  J A HUNT; V M INGRAM
Journal:  Nature       Date:  1958-04-12       Impact factor: 49.962

7.  The diagnosis of thalassemia trait by starch block electrophoresis of the hemoglobin.

Authors:  P S GERALD; L K DIAMOND
Journal:  Blood       Date:  1958-01       Impact factor: 22.113

8.  Observations on the inheritance of sickle-cell hemoglobin and hemoglobin C.

Authors:  H M RANNEY
Journal:  J Clin Invest       Date:  1954-12       Impact factor: 14.808

9.  Qualitative and quantitative control of adult hemoglobin synthesis; a multiple allele hypothesis.

Authors:  H A ITANO
Journal:  Am J Hum Genet       Date:  1953-03       Impact factor: 11.025

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
  10 in total
  1 in total

1.  HUMAN HEMOGLOBIN GENE LINKAGE: REPORT OF A FAMILY WITH HEMOGLOBIN B2, HEMOGLOBIN S, AND BETA THALASSEMIA, INCLUDING A PROBABLE CROSSOVER BETWEEN THALASSEMIA AND DELTA LOCI.

Authors:  H A PEARSON; M M MOORE
Journal:  Am J Hum Genet       Date:  1965-03       Impact factor: 11.025
  1 in total

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