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标记染色体:细胞遗传学特征及其对产前诊断的意义

Marker chromosomes: cytogenetic characterization and implications for prenatal diagnosis.

作者信息

Mohandas T, Canning N, Chu W, Passage M B, Anderson C E, Kaback M M

出版信息

Am J Med Genet. 1985 Feb;20(2):361-8. doi: 10.1002/ajmg.1320200220.

Abstract

Satellited marker chromosomes were identified in four individuals from unrelated families; one was first encountered in cultured amniotic fluid cells obtained for prenatal diagnostic studies. We present cytogenetic characterization of these marker chromosomes and clinical findings in the individuals carrying them. Identification of a marker chromosome in amniotic fluid cell cultures presents problems in genetic counseling, as it is often difficult to determine the clinical significance of such a finding. Chromosome-banding techniques now allow the precise identification of satellited marker chromosomes originating from chromosome 15. Presence of a supernumerary bisatellited der(15) marker chromosome containing the proximal long arm of 15 has been associated with mental and developmental retardation. Application of chromosome-banding techniques was useful in characterization of the marker chromosomes and providing prenatal genetic counseling.

摘要

在来自无亲缘关系家庭的4名个体中鉴定出了随体标记染色体;其中1例最初是在用于产前诊断研究而获取的羊水培养细胞中发现的。我们展示了这些标记染色体的细胞遗传学特征以及携带它们的个体的临床发现。在羊水细胞培养中鉴定出标记染色体给遗传咨询带来了问题,因为通常很难确定这一发现的临床意义。染色体显带技术现在能够精确鉴定源自15号染色体的随体标记染色体。含有15号染色体近端长臂的额外双随体der(15)标记染色体的存在与智力和发育迟缓有关。染色体显带技术的应用有助于标记染色体的特征描述并提供产前遗传咨询。

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