The prenatal detection of the fragile X chromosome: Review of recent experience-Reference-Cited by-同舟云学术

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

Published:1986-01 Issue:1-2 Volume:23 Page:297-311
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,Wilson Miriam G.,Lin Ming S.,Alfi Omar S.,Wassman E. Robert,Brooks Judith,Duncan Charlotte J.,Masia Annette,Krawczun Michael S.,Opitz John M.,Reynolds James F.

Publisher

Wiley

Subject

Genetics(clinical)

Reference42 articles.

1. (1985a): Genetic linkage heterogeneity in the fragile X syndrome. Hum Genet, in press.

2. Close linkage of fragile X-mental retardation syndrome to haemophilia B and transmission through a normal male

3. (1985): Fragile (X) expression induced by FUdR is transient and inversely related to levels of thymidylate synthase activity. Am J Hum Genet, in press.

Cited by 28 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. Fragile sites, chromosomal lesions, tandem repeats, and disease;Frontiers in Genetics;2022-11-17

2. Simultaneous expression of the rare and common fragile sites on the X chromosome;Clinical Genetics;2008-06-28

3. The common fragile site in band q27 of the human X chromosome is not coincident with the fragile X;Clinical Genetics;2008-06-28

4. Linkage analysis of the fragile X syndrome using a new DNA marker U6.2 defining locus DXS304;American Journal of Medical Genetics;1991-02-01

5. The fra(X) syndrome: Neurological, electrophysiological, and neuropathological abnormalities;American Journal of Medical Genetics;1991-02-01