Literature DB >> 6971621

Partial trisomy 20.

A Delicado, I Lopez Pajares, P Vicente, R Gracia.   

Abstract

A child with a facial dysmorphy and congenital malformations, showed in the chromosome analysis a partial trisomy of chromosome 20. This anomaly, resulted from a maternal translocation t(11;20), (q35;q11).

Entities:  

Mesh：

Year:  1981        PMID： 6971621

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


  2 in total

1.  Three new cases of partial monosomy 21 resulting from one ring 21 chromosome and two unbalanced reciprocal translocations.

Authors:  N Philip; M A Baeteman; M G Mattei; J F Mattei
Journal:  Eur J Pediatr       Date:  1984-04       Impact factor: 3.183

2.  The gene for bone morphogenetic protein 2A (BMP2A) is localized to human chromosome 20p12 by radioactive and nonradioactive in situ hybridization.

Authors:  V V Rao; C Löffler; J M Wozney; I Hansmann
Journal:  Hum Genet       Date:  1992-11       Impact factor: 4.132
  2 in total

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