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A search for uniparental disomy in carriers of supernumerary marker chromosomes.

作者信息

James R S, Temple I K, Dennis N R, Crolla J A

机构信息

Wessex Regional Genetics Laboratory, Salisbury District Hospital, UK.

出版信息

Eur J Hum Genet. 1995;3(1):21-6. doi: 10.1159/000472270.

DOI:10.1159/000472270
PMID:7767653
Abstract

As there is some evidence that individuals bearing supernumerary marker chromosomes (SMCs) might have an increased risk of being uniparentally disomic for the structurally normal homologues of the SMC, we made a systematic search for uniparental disomy of the autosomal homologues from which SMCs were derived. Of the 22 families studied, a biparental origin of the normal homologues was demonstrated in 21, and 1 case of paternal isodisomy of chromosome 6 was detected in the carrier of a supernumerary marker ring chromosome 6 which itself was of maternal origin. Our results confirm that uniparental disomy may be found in association with SMCs, but until more cases are studied we can only speculate on their frequency and the mechanism(s) which result in this phenomenon.

摘要

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引用本文的文献

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Supernumerary marker chromosomes derived from chromosome 6: cytogenetic, molecular cytogenetic, and array CGH characterization.6 号染色体衍生的额外标记染色体:细胞遗传学、分子细胞遗传学和 array CGH 特征分析。
Am J Med Genet A. 2012 Jul;158A(7):1568-73. doi: 10.1002/ajmg.a.35385. Epub 2012 May 25.
3
Molecular-cytogenetic characterization of the origin and the presence of pericentromeric euchromatin on minute supernumerary marker chromosomes (SMCs).
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Chromosome Res. 2004;12(3):239-44. doi: 10.1023/b:chro.0000021916.18019.1c.
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