Full Text Available
Note: Clicking the button above will open the full text document at the original institutional repository in a new window.
Significance of connexion genes in non-syndromic deafness in Africans
Includes abstract. Includes bibliographical references.
Saved in:
| Main Author: | |
|---|---|
| Other Authors: | |
| Format: | Thesis |
| Language: | English |
| Published: |
Division of Human Genetics
2014
|
| Tags: |
No Tags, Be the first to tag this record!
|
Similar Items: Significance of connexion genes in non-syndromic deafness in Africans
- Molecular analysis of GJB2 (connexin 26) and GJB6 (connexin 30) gene mutations in non-syndromic hereditary deafness in South Africa
- Delinquency and the family : a study of connexions between crime and socioenvironmental factors with special reference to inmates of the Constantia Reform School.
- Metabolic syndrome, the leptin gene and kidney disease in non-diabetic black South Africans
- Applying mixed models to assess gene significance with microarray data
- Deaf Parents’ Infant-Directed Touch with their Hearing and Deaf Babies: Intuitive, Cultural, or in Need of Instruction?
- Multimedia-Based Interventions to Improve Science Learning Outcomes for Deaf students at Wangsel Institute for the Deaf.