publication venue for
- A founder deletion in the TRPM1 gene associated with congenital stationary night blindness and myopia is highly prevalent in Ashkenazi Jews.. 6. 2019
- The Qatar genome: a population-specific tool for precision medicine in the Middle East.. 3. 2016
- Challenges in classifying human chromosomal heteromorphisms using banding cytogenetics: From controversial guidelines to the need for a universal scoring system. 2024