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婴儿自闭症中inv dup(15)染色体的母源起源

Maternal origin of inv dup(15) chromosomes in infantile autism.

作者信息

Martinsson T, Johannesson T, Vujic M, Sjöstedt A, Steffenburg S, Gillberg C, Wahlström J

机构信息

Department of Clinical Genetics, Göteborg University, East Hospital, Sweden.

出版信息

Eur Child Adolesc Psychiatry. 1996 Dec;5(4):185-92. doi: 10.1007/BF00538845.

Abstract

Six male patients with infantile autism and an extra inverted duplicated chromosome 15[inv dup(15)] were reported in a previous study. These patients had four copies of the chromosome region 15pter-q13, or an inv dup(15)(pter-->q13; q13-->pter). In this new study, DNA from the families of four of the patients were analysed using Southern based RFLPs and microsatellite polymorphisms from the region. In all four cases the inv dup(15) chromosome was of maternal origin. Furthermore, the data suggests that it originated in the maternal meiotic process rather than in an early mitosis in the developmental process of the embryo. The extra chromosome contained material from both of the maternally derived 15-chromosomes. Based on the molecular data presented here, a model for the origin of chromosome markers of this type is proposed.

摘要

先前的一项研究报告了6名患有婴儿自闭症且有一条额外倒位重复15号染色体[inv dup(15)]的男性患者。这些患者的染色体区域15pter-q13有四个拷贝,即inv dup(15)(pter→q13; q13→pter)。在这项新研究中,使用基于Southern的限制性片段长度多态性(RFLP)和该区域的微卫星多态性对其中4名患者家庭的DNA进行了分析。在所有4例中,inv dup(15)染色体均来自母亲。此外,数据表明它起源于母亲的减数分裂过程,而非胚胎发育过程中的早期有丝分裂。这条额外的染色体包含了两条来自母亲的15号染色体的物质。基于此处呈现的分子数据,提出了此类染色体标记起源的模型。

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