Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/9223
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Type: Journal article
Title: Recombinants of intrachromosomal transposition of subtelomeres in chromosomes 1 and 2: A cause of minute terminal chromosomal imbalances
Author: Daniel, A.
Baker, E.
Chia, N.
Haan, E.
Malafiej, P.
Hinton, L.
Clarke, N.
Ades, L.
Darmanian, A.
Callen, D.
Citation: American Journal of Medical Genetics. Part A, 2003; 117A(1):57-64
Publisher: Wiley-Liss
Issue Date: 2003
ISSN: 1552-4825
1552-4833
Statement of
Responsibility: 
Art Daniel, Elizabeth Baker, Nicole Chia, Eric Haan, Paul Malafiej, Lyn Hinton, Nigel Clarke, Lesley Adès, Artur Darmanian, and David Callen
Abstract: Two cases of submicroscopic recombinants of intrachromosomal transposition of telomeres, one each from chromosome 1 and 2 are described. Meiotic crossing-over would generate the recombinants from these reciprocal rearrangements. In both cases, which were detected by FISH with subtelomeric probes, there is a minute deletion of the qter region and a second presence of the pter subtelomeric region on the respective qter, i.e., a duplication of 1pter or 2pter respectively. The deletion on 2qter (case 2) was confirmed by microsatellite inheritance and was of paternal origin, but in case 1 there was no detectable 1q deletion other than of the subtelomeric probe, and parental origin could not be determined. The present case 2 with del(2qter)/dup(2pter) shares many features with reported cases of simple deletion (2qter) but did not have features of Albright hereditary osteodystrophy, which are seen in half of such deletion patients. The clinical features present in case 1 were similar to those of the previously reported case of a submicroscopic 1qter deletion but also to cases with microscopically visible 1qter deletions, presumably because of gene enrichment in subtelomeric regions. Recombinants of such intrachromosomal subtelomere transpositions detected by subtelomeric probes may comprise up to 10% of submicroscopic pter or qter deletion cases. Other cases of this unusual mechanism may be detected with more common use of subtelomeric probes. It is suggested the bouquet associations of telomeres in early meiosis may facilitate such unusual rearrangements.
Keywords: intrachromosomal subtelomere transposition; sub-telomeric probe; chromosome 1qter deletion; 2qter deletion
Description: © 2003 Wiley-Liss, Inc.
RMID: 0020030238
DOI: 10.1002/ajmg.a.10048
Published version: http://www3.interscience.wiley.com/cgi-bin/abstract/101519744/ABSTRACT?CRETRY=1&SRETRY=0
Appears in Collections:Medicine publications

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