New contributions to the study of common double mutants in the humanLDLreceptor gene
✍ Scribed by M. Teresa Tejedor; Ana Cenarro; Diego Tejedor; Marianne Stef; Lourdes Palacios; Isabel de Castro; Ángel L. García-Otín; Luis V. Monteagudo; Fernando Civeira; Miguel Pocovi
- Publisher
- Springer
- Year
- 2011
- Tongue
- English
- Weight
- 131 KB
- Volume
- 98
- Category
- Article
- ISSN
- 0028-1042
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
The case of a 2 1/2-month-old male child with intrauterine distrophy features and multiple congenital malformations is presented. Cytogenetic studies of the child and his parents, completed with Q- and G-banding techniques led us to conclude that it is a case of 22 trisomy inherited from his mother.
Fluctuation test5 2 la Luria and Delbruck were performed with mouse LMTK cells, and the result3 indicate that the appearance of variants resistant to cadmium i s due to random spontaneous mutations and not to epigenetic events. The rate of spontaneous mutations leading to cadmium resistance was calc