Fra(X) prenatal diagnosis: Are endoreduplicated and polyploid cells useful diagnostic criteria?
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference10 articles.
1. Prenatal diagnosis of fragile X syndrome
2. Distribution of diploidy, polyploidy, and endoreduplication in fra(X) positive and negative lymphocytes, amniocytes, and chorionic Villi
3. (1991b) Laboratory aspects of prenatal fra(X) detection. In (eds.): “Fragile X/Cancer Cytogenetics.” New York: Wiley-Liss, John Wiley & Sons, Inc.
Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Induction of micronuclei, hyperdiploidy and chromosomal breakage affecting the centric/pericentric regions of chromosomes 1 and 9 in human amniotic fluid cells after treatment with asbestos and ceramic fibers;Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis;1997-06-09
2. Rapid fragile X carrier screening and prenatal diagnosis using a nonradioactive PCR test;JAMA: The Journal of the American Medical Association;1993-10-06
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