Literature DB >> 5728677

Unusual chromosomal findings in a case of myelofibrosis.

R M Goodman, B A Bouroncle, F Miller, C North.   

Abstract

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Year:  1968        PMID： 5728677     DOI： 10.1093/oxfordjournals.jhered.a107742

Source DB:  PubMed          Journal:  J Hered        ISSN： 0022-1503            Impact factor:   2.645


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  2 in total

1.  Partial deletion of a group-F (19-20) chromosome in a physically handicapped psychiatric male patient.

Authors:  P Genest; M Bouchard; J Poty
Journal:  J Med Genet       Date:  1971-09       Impact factor: 6.318

2.  Ring F chromosome mosaicism (46,XY,20r-46,XY) in an epileptic child without apparent haematological disease.

Authors:  M Faed; H G Morton; J Robertson
Journal:  J Med Genet       Date:  1972-12       Impact factor: 6.318
  2 in total

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