Literature DB >> 5731934

Homozygous hereditary elliptocytosis as the cause of haemolytic anemia in infancy.

J A Nielsen, S Praktitioner.   

Abstract

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Year:  1968        PMID： 5731934     DOI： 10.1111/j.1600-0609.1968.tb00869.x

Source DB:  PubMed          Journal:  Scand J Haematol        ISSN： 0036-553X


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  3 in total

1.  Unique alpha-spectrin mutant in a kindred with common hereditary elliptocytosis.

Authors:  P A Lane; R L Shew; T A Iarocci; N Mohandas; T Hays; W C Mentzer
Journal:  J Clin Invest       Date:  1987-03       Impact factor: 14.808

2.  Camptobrachydactyly: a new autosomal dominant trait with two probable homozygotes.

Authors:  J A Edwards; R P Gale
Journal:  Am J Hum Genet       Date:  1972-07       Impact factor: 11.025

3.  Deficiency of skeletal membrane protein band 4.1 in homozygous hereditary elliptocytosis. Implications for erythrocyte membrane stability.

Authors:  G Tchernia; N Mohandas; S B Shohet
Journal:  J Clin Invest       Date:  1981-08       Impact factor: 14.808
  3 in total

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