六十六岁。“你测试过22q了吗?”

IF 3.5 2区 医学 Q2 GENETICS & HEREDITY
Peter Scambler
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引用次数: 0

摘要

1997年,医学遗传学杂志发表了我们关于与间质染色体22q11缺失相关的临床特征谱的论文。这种拷贝数变异与一系列临床特征有关,这导致了它最初与几种诊断标签的关联。自1997年以来,关于该综合征的临床和基础科学方面的工作以及减少为半合子的基因提供了有关最佳实践护理和潜在生物学的丰富信息。人们认识到22q11.2缺失综合征是探索精神疾病、心血管发展等潜在机制的极好模型。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Six at Sixty. 'Have you tested for 22q?'

In 1997, the Journal of Medical Genetics published our paper on the spectrum of clinical features associated with interstitial chromosome 22q11 deletions. This copy number variation is associated with an extraordinary range of clinical features, which led initially to its association with several diagnostic labels. Since 1997 work on clinical and basic science aspects of the syndrome and the genes reduced to hemizygosity have provided a wealth of information pertaining to both best practice care and underlying biology. It is recognised that 22q11.2 deletion syndrome is an excellent model for probing mechanisms underlying psychiatric disease, cardiovascular development and much more.

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来源期刊
Journal of Medical Genetics
Journal of Medical Genetics 医学-遗传学
CiteScore
7.60
自引率
2.50%
发文量
92
审稿时长
4-8 weeks
期刊介绍: Journal of Medical Genetics is a leading international peer-reviewed journal covering original research in human genetics, including reviews of and opinion on the latest developments. Articles cover the molecular basis of human disease including germline cancer genetics, clinical manifestations of genetic disorders, applications of molecular genetics to medical practice and the systematic evaluation of such applications worldwide.
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