The biochemical basis of sickle cell anemia in Saudi Arabia: A model case of genetic and molecular disorders
โ Scribed by AI Alayash; J Bonaventura
- Publisher
- Elsevier Science
- Year
- 1989
- Tongue
- English
- Weight
- 350 KB
- Volume
- 17
- Category
- Article
- ISSN
- 0307-4412
No coin nor oath required. For personal study only.
๐ SIMILAR VOLUMES
## Abstract **BACKGROUND:** Genetic skeletal disorders of the fetus and infant are a large group of genetic disorders, comprising the groups formerly assigned as skeletal dysplasias (osteochondrodysplasias), dysostoses, and malformation syndromes with a skeletal component. Genetic skeletal disorder
Neurofibromatosis type 1 (NF1) is a pleiotropic autosomal dominant disorder with marked variability of clinical expression. As in other heritable disorders, the mapping and cloning of the gene responsible for NF1 have increased our understanding of the pathogenesis of the condition. In particular, t