Author:
Jenkins Edmund C.,Sanz Maureen M.,Ray James H.,Stark-Houck Sandra L.,Brown W. Ted
Reference7 articles.
1. (1988) Clinical use of DNA markers in the fragile(X) syndrome for carrier detection and prenatal diagnosis. In (ed): “Nucleic Acid Probes in Diagnosis of Human Genetic Diseases.” New York: Alan R. Liss, Inc., pp 11-33.
2. C-anaphases in lymphocyte cultures versus premature centromere division syndromes
3. C-anaphases rediscovered
4. Frequency of tri- or multiradial configurations in fragile X identification
5. (1991) Improved prenatal detection of fra(X) (q27): Methods for prevention of false negatives in chorionic villus and amniotic fluid cell cultures. Am J Med Genet, this issue.
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