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Human Mutation|January 1, 1995
Molecular basis of late infantile metachromatic leukodystrophy in the Habbanite JewsJ Zlotogora, G Bach, C Bösenberg, et al.American Journal of Medical Genetics|March 1, 1984
Heterozygote detection in Hunter syndromeJ Zlotogora, G BachAmerican Journal of Medical Genetics|January 1, 1983
Deficiency of lysosomal hydrolases in apparently healthy individualsJ Zlotogora, G BachAmerican Journal of Human Genetics|February 1, 1986
Hunter syndrome: prenatal diagnosis in maternal serumJ Zlotogora, G BachHuman Genetics|February 1, 1995
A missense mutation P136L in the arylsulfatase A gene causes instability and loss of activity of the mutant enzymeS Kafert, U Heinisch, J Zlotogora, et al.American Journal of Human Genetics|January 1, 1995
Multiple mutations are responsible for the high frequency of metachromatic leukodystrophy in a small geographic areaU Heinisch, J Zlotogora, S Kafert, et al.American Journal of Human Genetics|February 1, 1988
Selection in favor of lysosomal storage disorders?J Zlotogora, M Zeigler, G BachPediatrics|June 1, 1987
Mucolipidosis type IV: clinical spectrum and natural historyN Amir, J Zlotogora, G BachHuman Mutation|January 1, 1994
Molecular genetics of metachromatic leukodystrophyV Gieselmann, J Zlotogora, A Harris, et al.American Journal of Human Genetics|September 1, 1980
Metachromatic leukodystrophy in the habbanite Jews: high frequency in a genetic isolate and screening for heterozygotesJ Zlotogora, G Bach, Y Barak, et al.Pageof 39