Authors: Mandel, H Szargel, R Labay, V Elpeleg, O Saada, A Shalata, A Anbinder, Y Berkowitz, D Hartman, C Barak, M Eriksson, S Cohen, N

Citation: H. Mandel et al., The deoxyguanosine kinase gene is mutated in individuals with depleted hepatocerebral mitochondrial DNA (vol 29, pg 337, 2001), NAT GENET, 29(4), 2001, pp. 491-491

Authors: Mandel, H Szargel, R Labay, V Elpeleg, O Saada, A Shalata, A Anbinder, Y Berkowitz, D Hartman, C Barak, M Eriksson, S Cohen, N

Citation: H. Mandel et al., The deoxyguanosine kinase gene is mutated in individuals with depleted hepatocerebral mitochondrial DNA, NAT GENET, 29(3), 2001, pp. 337-341

Authors: Sprecher, E Bergman, R Richard, G Lurie, R Shalev, S Petronius, D Shalata, A Anbinder, Y Leibu, R Perlman, I Cohen, N Szargel, R

Citation: E. Sprecher et al., Hypotrichosis with juvenile macular dystrophy is caused by a mutation in CDH3, encoding P-cadherin, NAT GENET, 29(2), 2001, pp. 134-136

Authors: Raz, T Labay, V Baron, D Szargel, R Anbinder, Y Barrett, T Rabl, W Viana, MB Mandel, H Baruchel, A Cayuela, JM Cohen, N

Citation: T. Raz et al., The spectrum of mutations, including four novel ones, in the thiamine-responsive megaloblastic anemia gene SLC19A2 of eight families, HUM MUTAT, 16(1), 2000, pp. 37-42

Authors: Shalata, A Mandel, H Dorche, C Zabot, MT Shalev, S Hugeirat, Y Arieh, D Ronit, Z Reiss, J Anbinder, Y Cohen, N

Citation: A. Shalata et al., Prenatal diagnosis and carrier detection for molybdenum cofactor deficiency type A in Northern Israel using polymorphic DNA markers, PRENAT DIAG, 20(1), 2000, pp. 7-11