Mutations or exclusion: an unusual case in paternity testing
β Scribed by A. Junge; B. Brinkmann; R. Fimmers; B. Madea
- Publisher
- Springer-Verlag
- Year
- 2005
- Tongue
- German
- Weight
- 83 KB
- Volume
- 120
- Category
- Article
- ISSN
- 0937-9827
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
Duchenne dystrophy (DMD) is an X-linked lethal condition which affects 1 in 3,500 boys. The DMD gene is deleted in about 60-65% of patients while in the remaining 35-40% the condition is caused by point mutations, small insertions, or duplications. We have ascertained 967 DMD families (680 isolated
The Werner's syndrome ( WS) is a rare recessive disease characterized by an early onset of geriatric disorders. The Werner's syndrome gene ( WRN), recently cloned, encodes for an helicase and therefore plays a role in DNA metabolism and DNA repair. Here, we report the study of a French family with t