Cohen M M, Rosenblum-Vos L S, Prabhakar G
Department of Pediatrics, University of Maryland School of Medicine, Baltimore.
Am J Dis Child. 1993 Nov;147(11):1159-66. doi: 10.1001/archpedi.1993.02160350033005.
Chromosomal abnormalities are the basis for a substantial proportion of human morbidity and mortality. During the past 35 years, the field of human cytogenetics has helped to elucidate the etiology of many congenital malformation/mental retardation syndromes. Through adaptation of technological advances and integration of molecular biological techniques, cytogenetics continues to contribute significantly to our knowledge of clinical genetics, chromosomal fine structure and function, gene mapping, and prenatal diagnosis. This review outlines the basic concepts, recent findings, and current laboratory approaches to cytogenetic diagnosis.
染色体异常是导致人类大量发病和死亡的重要原因。在过去35年里,人类细胞遗传学领域有助于阐明许多先天性畸形/智力发育迟缓综合征的病因。通过采用技术进步并整合分子生物学技术,细胞遗传学继续为我们在临床遗传学、染色体精细结构与功能、基因定位及产前诊断等方面的知识做出重大贡献。本综述概述了细胞遗传学诊断的基本概念、最新发现及当前实验室方法。