Mosaic inversion duplication of chromosome 15 without phenotypic effect: Occurrence in a father and daughter

1 March 1984

journal article
case report
Published by Wiley in American Journal of Medical Genetics

Vol. 17 (3) , 649-654
https://doi.org/10.1002/ajmg.1320170315

Abstract

A mosaic marker chromosome was observed in 2 generations. Multiple staining techniques identified it as an inverted duplication of chromosome 15 (inv dup 15) derived from the paternal grandmother. Although this inv dup 15 included a central R band, there was no noticeable phenotypic effect.

Keywords

This publication has 8 references indexed in Scilit:

Supernumerary chromosomes in six patients
Clinical Genetics, 2008
Prenatal detection of an accessory chromosome identified as an inversion duplication (15)
Human Genetics, 1981
Preferential maternal derivation in inv dup(15)
Human Genetics, 1981
Properties and significance of a small marker chromosome in amniotic fluid cells
Clinical Genetics, 1980
An extra idic(15p)(q11) chromosome in Prader-Willi syndrome
Human Genetics, 1980
Prader‐Willi syndrome and a bisatellited derivative of chromosome 15
Clinical Genetics, 1980
Cytogenetic and clinical studies in five cases of inv dup(15)
Human Genetics, 1979
Preferential derivation of abnormal human G-group-like chromosomes from chromosome 15
Human Genetics, 1977