Literature DB >> 468256

A chromosomal abnormality (21q-) in primary thrombocytosis.

P Petit, H Van den Berghe.   

Abstract

A patient with thrombocytosis was found to present an acquired deletion of the long arm of chrosome 21 (21q-). A similar observation reported in the literature is hereby confirmed.

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Mesh：

Year:  1979        PMID： 468256     DOI： 10.1007/bf00295597

Source DB:  PubMed          Journal:  Hum Genet        ISSN： 0340-6717            Impact factor:   4.132


  1 in total

1.  A chromosomal abnormality in primary thrombocythemia.

Authors:  A Zaccaria; S Tura
Journal:  N Engl J Med       Date:  1978-06-22       Impact factor: 91.245
  1 in total
  2 in total

1.  Acute transformation of essential thrombocythaemia: report of two cases.

Authors:  A M O'Hea; W Erber; N T O'Connor; C Bunch
Journal:  J Clin Pathol       Date:  1986-12       Impact factor: 3.411

2.  Acute lymphocytic and myelomonocytic leukemia associated with low platelet counts and a 21q- marker chromosome.

Authors:  G Alimena; B Dallapiccola; M R De Cuia; F Mandelli; F Mitelman
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132
  2 in total

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