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使用亚端粒探针研究智力迟钝。

The use of subtelomeric probes to study mental retardation.

作者信息

Knight Samantha J L, Flint Jonathan

机构信息

The Wellcome Trust Centre for Human Genetics, Churchill Hospital, Headington, Oxford, Oxfordshire OX3 7BN, United Kingdom.

出版信息

Methods Cell Biol. 2004;75:799-831. doi: 10.1016/s0091-679x(04)75035-9.

Abstract

In this chapter, we focus on the genetic basis of mental retardation (MR), specifically the use of subtelomeric probes to provide new diagnoses in idiopathic MR. We discuss both the background to the clinical demand for diagnoses and the technological advances that culminated in the development of subtelomeric testing strategies. We explain the theory behind these strategies and briefly outline the protocols involved, giving the advantages, limitations, and pitfalls of the analyses. Finally, we give an overview of the MR subtelomeric studies to date and how subtelomeric testing has become a widely used tool in clinical diagnostic laboratories, particularly in the diagnosis of unexplained MR, but also in other fields of clinical medicine. The conclusion addresses the overall impact that subtelomeric testing has had on the diagnosis of MR, the implications for patients and their families, and future research avenues for exploring the genetic causes of MR and improving our overall understanding of neurocognitive development.

摘要

在本章中,我们重点关注智力迟钝(MR)的遗传基础,特别是使用亚端粒探针为特发性MR提供新的诊断方法。我们将讨论临床诊断需求的背景以及最终促成亚端粒检测策略发展的技术进步。我们解释这些策略背后的理论,并简要概述所涉及的方案,阐述分析的优点、局限性和陷阱。最后,我们概述了迄今为止的MR亚端粒研究,以及亚端粒检测如何成为临床诊断实验室中广泛使用的工具,特别是在不明原因MR的诊断中,也在临床医学的其他领域中。结论部分阐述了亚端粒检测对MR诊断的总体影响、对患者及其家庭的意义,以及探索MR遗传原因和增进我们对神经认知发育整体理解的未来研究途径。

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