Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

E L Aronovich

Showing results (1-10 of 17) with videos related to

Pageof 2
Sort By:
American Journal of Human Genetics|January 1, 1996
Molecular genetic defect underlying alpha-L-iduronidase pseudodeficiencyE L Aronovich, D Pan, C B Whitley
Biokhimiia (Moscow, Russia)|January 1, 1990
[Isolation and characteristics of hexosaminidase A and activator protein from human kidney]E L Aronovich, V S Akhunov, K D Krasnopol'skaia
Voprosy Meditsinskoi Khimii|May 1, 1982
[Use of lysosome enzymes in genetic counseling]K D Krasnopol'skaia, E L Aronovich, S M Terekhov
American Journal of Human Genetics|March 7, 1998
Genotype-phenotype correspondence in Sanfilippo syndrome type BH G Zhao, E L Aronovich, C B Whitley
American Journal of Human Genetics|March 1, 1995
Molecular diagnosis of mucopolysaccharidosis type II (Hunter syndrome) by automated sequencing and computer-assisted interpretation: toward mutation mapping of the iduronate-2-sulfatase geneJ J Jonsson, E L Aronovich, S E Braun, et al.
Genetika|August 1, 1986
[Detection of homozygotes and heterozygote carriers of GM2-gangliosidosis]E L Aronovich, K D Krasnopol'skaia, V I Kukharenko, et al.
Genetika|October 1, 1989
[Study of the genetic heterogeneity of gangliosidoses in humans]V S Akhunov, E L Aronovich, K D Krasnopol'skaia, et al.
Genomics|June 21, 2001
Molecular basis of mucopolysaccharidosis type IIIB in emu (Dromaius novaehollandiae): an avian model of Sanfilippo syndrome type BE L Aronovich, J M Johnston, P Wang, et al.
Voprosy Meditsinskoi Khimii|July 1, 1988
[Prenatal diagnosis of hereditary lysosomal diseases]T V Mirenburg, E L Aronovich, T V Lebedeva, et al.
Human Gene Therapy|February 10, 1996
Preclinical studies of lymphocyte gene therapy for mild Hunter syndrome (mucopolysaccharidosis type II)S E Braun, D Pan, E L Aronovich, et al.
Pageof 2

Showing results (1-10 of 17) with videos related to

Sort By:
Pageof 2
American Journal of Human Genetics|January 1, 1996
Molecular genetic defect underlying alpha-L-iduronidase pseudodeficiencyE L Aronovich, D Pan, C B Whitley
Biokhimiia (Moscow, Russia)|January 1, 1990
[Isolation and characteristics of hexosaminidase A and activator protein from human kidney]E L Aronovich, V S Akhunov, K D Krasnopol'skaia
Voprosy Meditsinskoi Khimii|May 1, 1982
[Use of lysosome enzymes in genetic counseling]K D Krasnopol'skaia, E L Aronovich, S M Terekhov
American Journal of Human Genetics|March 7, 1998
Genotype-phenotype correspondence in Sanfilippo syndrome type BH G Zhao, E L Aronovich, C B Whitley
American Journal of Human Genetics|March 1, 1995
Molecular diagnosis of mucopolysaccharidosis type II (Hunter syndrome) by automated sequencing and computer-assisted interpretation: toward mutation mapping of the iduronate-2-sulfatase geneJ J Jonsson, E L Aronovich, S E Braun, et al.
Genetika|August 1, 1986
[Detection of homozygotes and heterozygote carriers of GM2-gangliosidosis]E L Aronovich, K D Krasnopol'skaia, V I Kukharenko, et al.
Genetika|October 1, 1989
[Study of the genetic heterogeneity of gangliosidoses in humans]V S Akhunov, E L Aronovich, K D Krasnopol'skaia, et al.
Genomics|June 21, 2001
Molecular basis of mucopolysaccharidosis type IIIB in emu (Dromaius novaehollandiae): an avian model of Sanfilippo syndrome type BE L Aronovich, J M Johnston, P Wang, et al.
Voprosy Meditsinskoi Khimii|July 1, 1988
[Prenatal diagnosis of hereditary lysosomal diseases]T V Mirenburg, E L Aronovich, T V Lebedeva, et al.
Human Gene Therapy|February 10, 1996
Preclinical studies of lymphocyte gene therapy for mild Hunter syndrome (mucopolysaccharidosis type II)S E Braun, D Pan, E L Aronovich, et al.
Pageof 2