Literature DB >> 3239578

Deletion 9p, duplication 18q in two sisters resulting from a maternal (9;18) (p22;q21.3) translocation.

S M Tayel1, T W Kurczynski, S Casperson, M M McCorquodale.   

Abstract

We have studied two sisters with partial deletion 9p and partial duplication 18q resulting from adjacent 1 segregation of a maternal translocation (9;18) (p22;q21.3). The clinical manifestations identified in our patients were compared with those reported in the literature for 9p- and 18q+ patients involving approximately the same amount of genetic material. There was relatively greater similarity with the 9p- syndrome than with dup (18q) syndrome, but typical characteristics of both conditions were lacking.

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Year:  1988        PMID: 3239578     DOI: 10.1002/ajmg.1320310419

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  2 in total

Review 1.  Clinical and molecular evaluation of four patients with partial duplications of the long arm of chromosome 18.

Authors:  R Mewar; A D Kline; W Harrison; K Rojas; F Greenberg; J Overhauser
Journal:  Am J Hum Genet       Date:  1993-12       Impact factor: 11.025

2.  Molecular definition of a chromosome 9p21 germ-line deletion in a woman with multiple melanomas and a plexiform neurofibroma: implications for 9p tumor-suppressor gene(s).

Authors:  E M Petty; L H Gibson; J W Fountain; J L Bolognia; T L Yang-Feng; D E Housman; A E Bale
Journal:  Am J Hum Genet       Date:  1993-07       Impact factor: 11.025

  2 in total

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