Tuffery S, Moine P, Sarda P, Lefort G, Boulot P, Demaille J, Claustres M
Laboratoire de Biochimie Génétique, CNRS UPR 9008/CRBM U249 INSERM, Institut de Biologie, Montpellier, France.
Genet Couns. 1994;5(2):183-5.
We report the molecular diagnosis of Duchenne muscular dystrophy (DMD) in an extended pedigree by use of a conformational polymorphism detected by the SSCP method, which allowed direct prenatal diagnosis and carrier detection while no DNA from an affected boy was available.
我们报告了一个通过使用SSCP方法检测到的构象多态性,对一个大家族进行杜氏肌营养不良症(DMD)分子诊断的案例。在没有患病男孩DNA的情况下,该方法实现了直接的产前诊断和携带者检测。