𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Mutation detection 2001: Novel technologies, developments and applications for analysis of the human genome

✍ Scribed by Richard G.H. Cotton


Publisher
John Wiley and Sons
Year
2002
Tongue
English
Weight
135 KB
Volume
19
Category
Article
ISSN
1059-7794

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


Evaluation and application of denaturing
✍ GΓ‘bor MΓ‘tyΓ‘s; Anne De Paepe; Dorothy Halliday; Catherine Boileau; Gerard Pals; B πŸ“‚ Article πŸ“… 2002 πŸ› John Wiley and Sons 🌐 English βš– 571 KB

## Communicated by Darwin Prockop Mutations in the human fibrillin 1 gene (FBN1) cause the Marfan syndrome (MFS), an autosomal dominant connective tissue disorder. Knowledge about FBN1 mutations is important for early diagnosis, management, and genetic counseling. However, mutation detection in FB

Optimization of a simple and rapid singl
✍ Yolanda Espinosa-Parrilla; Marta Morell; Montserrat Borrell; Joan Carles Souto; πŸ“‚ Article πŸ“… 2000 πŸ› John Wiley and Sons 🌐 English βš– 448 KB πŸ‘ 2 views

Anticoagulant protein S (PS) deficiency is a known risk factor for thrombophilia. The structure and high allelic heterogeneity of the PS gene (PROS1), together with the presence of a 97% homologous pseudogene, complicates PROS1 analysis. We have optimized a simple, fast, and non-isotopic Single-Stra