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Case report: uniparental disomy 16 in association with congenital heart disease.

作者信息

O'Riordan S, Greenough A, Moore G E, Bennett P, Nicolaides K H

机构信息

Department of Child Health, King's College Hospital, London, U.K.

出版信息

Prenat Diagn. 1996 Oct;16(10):963-5. doi: 10.1002/(SICI)1097-0223(199610)16:10<963::AID-PD982>3.0.CO;2-S.

DOI:10.1002/(SICI)1097-0223(199610)16:10<963::AID-PD982>3.0.CO;2-S
PMID:8938071
Abstract

Uniparental disomy (UPD) is the inheritance of both copies of a given chromosome from the same parent (Warburton, 1988; Anon., 1991). The exact disease associations of UPD of individual chromosomes have yet to be fully elucidated and the question of whether UPD of some chromosomes may be regarded as a benign finding remains unanswered. We report an infant with uniparental maternal disomy 16, the only such infant identified at King's College Hospital. The infant had intrauterine growth retardation and minor congenital heart disease.

摘要

相似文献

1
Case report: uniparental disomy 16 in association with congenital heart disease.
Prenat Diagn. 1996 Oct;16(10):963-5. doi: 10.1002/(SICI)1097-0223(199610)16:10<963::AID-PD982>3.0.CO;2-S.
2
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Comprehensive 4-year follow-up on a case of maternal heterodisomy for chromosome 16.对一例16号染色体母源异二体病例的4年综合随访。
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Maternal uniparental disomy for chromosome 14 in a boy with intrauterine growth retardation.一名患有宫内生长迟缓男孩的母源14号染色体单亲二体。
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Evidence for imprinting on chromosome 16: the effect of uniparental disomy on the outcome of mosaic trisomy 16 pregnancies.16号染色体印记的证据:单亲二体对嵌合型16三体妊娠结局的影响。
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引用本文的文献

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Inherited surfactant deficiency caused by uniparental disomy of rare mutations in the surfactant protein-B and ATP binding cassette, subfamily a, member 3 genes.由表面活性蛋白-B 和 ATP 结合盒,亚家族 A,成员 3 基因中的罕见突变引起的单亲二体性导致的遗传性表面活性剂缺乏症。
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Maternal uniparental disomy of chromosome 16 in a case of spontaneous abortion.
一例自然流产病例中染色体16的母源单亲二体。
J Hum Genet. 2004;49(4):177-181. doi: 10.1007/s10038-004-0128-5. Epub 2004 Mar 2.