Literature DB >> 920172

Trisomy 20 mosaicism.

X Carbonell, M R Caballin, A Rubio, J Egozcue.   

Abstract

The first known case of trisomy 20 mosaicism is described. As in other cases of (partial) trisomy 20, the patient showed scarce physical malformations. It is suggested that trisomies for chromosomes of the F group are rare not because they are lethal but as a result of the morphology of the chromosomes involved.

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Year:  1977        PMID: 920172     DOI: 10.1111/j.1651-2227.1977.tb07990.x

Source DB:  PubMed          Journal:  Acta Paediatr Scand        ISSN: 0001-656X


  2 in total

1.  Trisomy 20pter = to q11 in a malformed boy from a t(13;20)(p11;q11) translocation-carrier mother.

Authors:  A Schinzel
Journal:  Hum Genet       Date:  1980-02       Impact factor: 4.132

2.  On the significance of true trisomy 20 mosaicism in amniotic fluid culture.

Authors:  M Djalali; P Steinbach; E Schwinger; G Schwanitz; U Tettenborn; M Wolf
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

  2 in total

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