How can the frequency of false-negative findings in prenatal diagnoses of fra(X) be reduced: Experience with first trimester chorionic Villi sampling
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference20 articles.
1. Multilocus analysis of the fragile X syndrome
2. Isolation of a DNA probe of potential use for diagnosis of the fragile-X syndrome
3. Recent experience in prenatal fra(X) detection
Cited by 4 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. Molekulargenetische Grundlagen des fra(X)-Syndroms—Diagnostik und therapeutische Hilfen;Monogen bedingte Erbkrankheiten 1;2000
2. Nuclear and chromosomal replication patterns in chorionic villi cells by bromodeoxyuridine labelling and DNA flow cytometry;Cell Proliferation;1992-07
3. Prenatal diagnosis and carrier detection in fragile X;American Journal of Medical Genetics;1992-04-15
4. Instability of a 550-Base Pair DNA Segment and Abnormal Methylation in Fragile X Syndrome;Science;1991-05-24
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