Specific molecular prenatal diagnosis for the CTG mutation in myotonic dystrophy.
Myring, J; Meredith, A L; Harley, H G; Kohn, G; Norbury, G; Harper, P S; Shaw, D J
- 期刊名称Journal of Medical Genetics
- 作者Myring, J; Meredith, A L; Harley, H G; Kohn, G; Norbury, G; Harper, P S; Shaw, D J
- 卷第29卷
- 期第11期
- 电子ISSN1468-6244
- 文件大小889.32KB
- 发表时间1992-11-01
- DOI10.1136/jmg.29.11.785
- 页码785-788