Literature DB >> 6982674

Recombinant chromosome 18 in two offspring of a chromosome 18 inversion heterozygote.

T Andrews, A C Gardiner, A R Boon.   

Abstract

A case of partial trisomy of chromosome 18 due to a recombinant pericentric inversion is described. Prenatal diagnosis in a subsequent pregnancy identified a foetus with the recombinant chromosome 18, and the pregnancy was terminated. A comparison is made between the risks reported in the relevant literature where recombinant offspring have resulted from chromosome 18 inversion heterozygotes and those observed in this case.

Mesh：

Year:  1982        PMID： 6982674

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


  3 in total

1.  A Peruvian Child with 18p-/18q+ Syndrome and Persistent Microscopic Hematuria.

Authors:  Julio A Poterico; Flor Vásquez; Miguel Chávez-Pastor; Milana Trubnykova; Félix Chavesta; Jenny Chirinos; Nancy Salcedo; Rosmery Mena; Sulema Cubas; Rocío González; Rossana Alvariño; Hugo Abarca-Barriga
Journal:  J Pediatr Genet       Date:  2017-07-06

2.  Monosomy 18p and pure trisomy 18p in a family with translocation (7;18).

Authors:  M Habedank; G Trost-Brinkhues
Journal:  J Med Genet       Date:  1983-10       Impact factor: 6.318

3.  Pericentric inversion of chromosome 18 in parents leading to a phenotypically normal child with segmental uniparental disomy 18.

Authors:  Ariana Kariminejad; Roxana Kariminejad; Azadeh Moshtagh; Maryam Zanganeh; Mohammad Hassan Kariminejad; Stefan Neuenschwander; Michal Okoniewski; Eva Wey; Albert Schinzel; Alessandra Baumer
Journal:  Eur J Hum Genet       Date:  2011-02-16       Impact factor: 4.246
  3 in total

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