Fragile X syndrome screening of families with consanguineous and non-consanguineous parents in the Iranian population
β Scribed by Ali Reza Pouya; Seyedeh Sedigheh Abedini; Neda Mansoorian; Farkhondeh Behjati; Nooshin Nikzat; Marzieh Mohseni; Sahar Esmaeeli Nieh; Lia Abbasi Moheb; Hossein Darvish; Gholamreza Bahrami Monajemi; Susan Banihashemi; Kimia Kahrizi; Hans Hilger Ropers; Hossein Najmabadi
- Book ID
- 116433181
- Publisher
- Elsevier Science
- Year
- 2009
- Tongue
- English
- Weight
- 106 KB
- Volume
- 52
- Category
- Article
- ISSN
- 1769-7212
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
## Communicated by Henrik Dahl Approximately 80% of hereditary hearing loss is non-syndromic. Non-syndromic deafness is the most genetically heterogeneous trait. The most common and severe form of hereditary hearing impairment is autosomal recessive non-syndromic hearing loss (ARNSHL), accounting f
This study examined the relationship between diagnosis, experience with insurance underwriting, and perceptions of difficulties with insurance in genetically tested families. Discrimination was strictly defined as the misuse of genetic information in underwriting. Forty-eight families received a sur