Fragile X induction systems in CVS cultures: Effect on cytogenetic, PCR, and genomic southern blot DNA analyses of the FMR-1 gene-Reference-Cited by-同舟云学术

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Fragile X induction systems in CVS cultures: Effect on cytogenetic, PCR, and genomic southern blot DNA analyses of the FMR-1 gene

Published:1994-07-15 Issue:4 Volume:51 Page:436-442
ISSN:0148-7299
Container-title:American Journal of Medical Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Jenkins Edmund C.,Morys Iwana,Henderson Jeanine,Genovese Marilyn,Carter Mary,Li Shu-Yun,Houck George E.,Ding Xiaohua,Stark-Houck Sandra L.,Dobkin Carl S.,Brown W. Ted

Publisher

Wiley

Subject

Genetics(clinical)

Reference8 articles.

1. Rapid Fragile X Carrier Screening and Prenatal Diagnosis Using a Nonradioactive PCR Test

2. Prenatally detected fragile X females: Long-term follow-up studies show high risk of mental impairment

3. Improved prenatal detection of fra(X)(q27.3): Methods for prevention of false negatives in chorionic villus and amniotic fluid cell cultures

4. Prenatally detected fragile X females: Long-term follow-up studies show high risk of mental impairment

5. (1992b): Prenatal diagnosis of the fragile X syndrome. In (ed): “Genetic Disorders of the Fetus.” Baltimore: Johns Hopkins University Press, pp 241-255.

Cited by 1 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. Screening for Fragile X Syndrome: Information Needs for Health Planners;Journal of Medical Screening;1997-06

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