Literature DB >> 314256

A cascade of chromosomal aberrations in three generations: a fragile 16q, an extra fragment and a rearranged 20.

G B Côté, S Papadakou-Lagoyanni, S Pantelakis.   

Abstract

The propositus' grandmother has a fragile 16q and belongs to a large family where several abortions and congenital anomalies were recorded. The portion distal to the fragile site was inherited as an extra fragment by the proposius' father who has it in 11% of his lymphocyte metaphases. This phenotypically harmless fragment has a high affinity for satellited chromosomes and was probably a main factor in the causation of the rearrangement that produced the partial trisomy 20p found in the propositus.

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Year:  1978        PMID: 314256

Source DB:  PubMed          Journal:  Ann Genet        ISSN: 0003-3995


  2 in total

1.  Fragile chromosome 16(q22) cause a balanced translocation at the same point.

Authors:  J M García-Sagredo; C San Román; M E Gallego Gómez; G Lledo
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

2.  The fragile site on chromosome 16 (q21q22). Data on four new families.

Authors:  F Shabtai; S Bichacho; I Halbrecht
Journal:  Hum Genet       Date:  1980       Impact factor: 4.132

  2 in total

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