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