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Specific molecular prenatal diagnosis for the CTG mutation in myotonic dystrophy.

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
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