R. Parvari
Genetics Institute Soroka Medical Center
Beer Sheva
Israel
Name/email consistency: low
- Homozygosity and linkage-disequilibrium mapping of the syndrome of congenital hypoparathyroidism, growth and mental retardation, and dysmorphism to a 1-cM interval on chromosome 1q42-43. Parvari, R., Hershkovitz, E., Kanis, A., Gorodischer, R., Shalitin, S., Sheffield, V.C., Carmi, R. Am. J. Hum. Genet. (1998)
- Two new mutations in the glucose-6-phosphatase gene cause glycogen storage disease in Hungarian patients. Parvari, R., Lei, K.J., Szonyi, L., Narkis, G., Moses, S., Chou, J.Y. Eur. J. Hum. Genet. (1997)
- A single-base deletion in the 3'-coding region of glycogen-debranching enzyme is prevalent in glycogen storage disease type IIIA in a population of North African Jewish patients. Parvari, R., Moses, S., Shen, J., Hershkovitz, E., Lerner, A., Chen, Y.T. Eur. J. Hum. Genet. (1997)