Reference38 articles.
1. Adachi, M., Schneck, L., & Volk, B. W. (1974). Ultrastructural studies of eight cases of fetal Tay-Sachs disease. Laboratory Investigation, 30, 102–112.
2. Akli, S., Boue, J., Sandhoff, K., et al. (1993). Collaborative study of the molecular epidemiology of Tay-Sachs disease in Europe. European Journal of Human Genetics, 1, 229–238.
3. Argov, Z., & Navon, R. (1984). Clinical and genetic variations in the syndrome of adult GM2 gangliosidosis resulting from hexosaminidase A deficiency. Annals of Neurology, 16, 14–20.
4. Aydin, K., Bakir, B., Tatli, B., et al. (2005). Proton MR spectroscopy in three children with Tay-Sachs disease. Pediatric Radiology, 35, 1081–1085.
5. Bach, G., Tomczak, J., Risch, N., et al. (2001). Tay-Sachs screening in the Jewish Ashkenazi population: DNA testing is the preferred procedure. American Journal of Medical Genetics, 99(1), 70–75.
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