Literature DB >> 5100207

The May-Hegglin anomaly: ultrastructure of the granulocytic inclusion.

E H Jenis, A Takeuchi, D E Dillon, F B Ruymann, S Rivkin.   

Abstract

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Year:  1971        PMID： 5100207     DOI： 10.1093/ajcp/55.2.187

Source DB:  PubMed          Journal:  Am J Clin Pathol        ISSN： 0002-9173            Impact factor:   2.493


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  2 in total

1.  The gene for May-Hegglin anomaly localizes to a <1-Mb region on chromosome 22q12.3-13.1.

Authors:  J A Martignetti; K E Heath; J Harris; N Bizzaro; A Savoia; C L Balduini; R J Desnick
Journal:  Am J Hum Genet       Date:  2000-03-17       Impact factor: 11.025

2.  Hereditary types of thrombocytopenia with giant platelets and inclusion bodies in the leukocytes.

Authors:  A Greinacher; C Mueller-Eckhardt
Journal:  Blut       Date:  1990-02
  2 in total

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