Literature DB >> 8494030

Trisomy 22 confirmed by fluorescent in situ hybridization.

R F Stratton1, B R DuPont, V L Mattern, R S Young, J W McCourt, C M Moore.   

Abstract

We report on a newborn girl with multiple congenital anomalies, whose G-banded chromosome analysis showed complete trisomy 22. Chromosome painting using a whole-chromosome painting probe for chromosome 22 confirmed that neither chromosome 22 was involved in a cryptic translocation.

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Year:  1993        PMID: 8494030     DOI: 10.1002/ajmg.1320460119

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


  2 in total

1.  Partial trisomy 22 (q11.2-q13.1) as a result of duplication and pericentric inversion.

Authors:  V P Prasher; E Roberts; A Norman; A C Butler; V H Krishnan; D J McMullan
Journal:  J Med Genet       Date:  1995-04       Impact factor: 6.318

2.  Live-born trisomy 22: patient report and review.

Authors:  T Heinrich; I Nanda; M Rehn; U Zollner; E Frieauff; J Wirbelauer; T Grimm; M Schmid
Journal:  Mol Syndromol       Date:  2013-01-11
  2 in total

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