The opinions or assertions contained herein are the private views of the authors, and are not to be construed as official or reflecting the views of the Department of the Army or the Department of Defense.
Hemoglobin southampton (Casper): Characterization of the base mutation
β Scribed by Nicholas H. Heintz; Dr. Phillip L. Howard
- Publisher
- John Wiley and Sons
- Year
- 1989
- Tongue
- English
- Weight
- 316 KB
- Volume
- 30
- Category
- Article
- ISSN
- 0361-8609
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
a-Thalassemia is usually due to deletions within the a-globin gene cluster, leading to loss of function of one ( -U ) or both [ -( a ) or --I a-globin genes. Nondeletion mutations (denoted a m T or a' . ) are less frequent and in Greece are not well defined. We report the analysis of 16 nondeletion
Direct sequencing analysis is largely used to confirm and characterize mutations previously detected by more rapid tests. We have developed a method-Comparative Sequence Analysis (CSA)that simplifies the analysis of sequencing data facilitating its use as a first screen for mutation detection. Seque
## Abstract For Abstract see ChemInform Abstract in Full Text.
Polychaete species belonging to the genus Branchipolynoe are commensal with mussels from deep-sea hydrothermal vents and cold-seeps. Possessing hemoglobins (Hbs), the species B. symmytilida, which is found in the mussel Bathymodiolus thermophilus on the East Pacific Rise, is exceptional in a family