Recent experience in prenatal fra(X) detection-Reference-Cited by-同舟云学术

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Recent experience in prenatal fra(X) detection

Published:1988-05 Issue:1-2 Volume:30 Page:329-336
ISSN:0148-7299
Container-title:American Journal of Medical Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Jenkins Edmund C.,Brown W. Ted,Krawczun Michael S.,Duncan Charlotte J.,Lele Kusum P.,Cantu Eduardo S.,Schonberg Steven,Golbus Mitchell S.,Sekhon Gurbax S.,Stark Sandra,Kunaporn Suphat,Silverman Wayne P.

Publisher

Wiley

Subject

Genetics (clinical)

Reference11 articles.

1. Further evidence for genetic heterogeneity in the fragile X syndrome

2. (1988): Multipoint linkage of 9 anonymous probes to HPRT, factor 9, and fragile X. This issue.

3. The prenatal detection of the fragile X chromosome: Review of recent experience

4. (1987): Personal communication.

Cited by 17 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. Recent advances in assays for the fragile X-related disorders;Human Genetics;2017-09-02

2. Cytogenetic experience in prenatal fra(X) detection on amniotic fluid cultures;Prenatal Diagnosis;1992-07

3. Nuclear and chromosomal replication patterns in chorionic villi cells by bromodeoxyuridine labelling and DNA flow cytometry;Cell Proliferation;1992-07

4. Recent experience in prenatal diagnosis of fragile X;American Journal of Medical Genetics;1992-04-15

5. Prenatal diagnosis of genetic disease;Fresenius' Journal of Analytical Chemistry;1992

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