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I Liebaers

Showing results (11-20 of 211) with videos related to

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Comptes Rendus Des Seances De La Societe De Biologie Et De Ses Filiales|January 1, 1973
[Separation of hexosaminidase isoenzymes in normal leukocytes, cultured fibroblasts and amniotic fluid cells: demonstration of 3 fractions]I Liebaers, E Vamos, I M Mandelbaum
Acta Clinica Belgica|January 1, 1974
Study of the beta-bexosyminidase separation by electrophoresis in homozygote and heterozygote Tay-Sachs cultured fibroblastsI Liebaers, E Vamos, I M Mandelbaum
Molecular and Cellular Endocrinology|March 20, 2002
Intracytoplasmic sperm injectionAndré Van Steirteghem, P Devroey, I Liebaers
Human Genetics|January 28, 1999
A mutation (IVS8+0.6kbdelTC) creating a new donor splice site activates a cryptic exon in an Alu-element in intron 8 of the human beta-glucuronidase geneR Vervoort, R Gitzelmann, W Lissens, et al.
Human Reproduction (Oxford, England)|September 28, 2002
Epigenetic risks related to assisted reproductive technologies: risk analysis and epigenetic inheritanceM De Rycke, I Liebaers, A Van Steirteghem
Advances in Experimental Medicine and Biology|January 1, 1976
Iduronate sulfatase determination for the diagnosis of the Hunter syndrome and the detection of the carrier stateE F Neufeld, I Liebaers, T W Lim
Biochemical and Biophysical Research Communications|May 31, 1982
Biochemical characterization of neonatal multiple sulfatase deficient (MSD) disorder cultured skin fibroblastsY Eto, T Tokoro, I Liebaers, et al.
The Journal of Pediatrics|March 1, 1977
Iduronate sulfatase in amniotic fluid: an aid in the prenatal diagnosis of the hunter syndromeI Liebaers, P Di Natale, E F Neufeld
Urologia Internationalis|August 8, 2001
DNA methylation analysis in immature testicular sperm cells at different developmental stagesM Manning, W Lissens, W Weidner, et al.
Human Genetics|March 1, 1992
Pyruvate dehydrogenase (PDH) deficiency caused by a 21-base pair insertion mutation in the E1 alpha subunitL De Meirleir, W Lissens, E Vamos, et al.
Pageof 22

Showing results (11-20 of 211) with videos related to

Sort By:
Pageof 22
Comptes Rendus Des Seances De La Societe De Biologie Et De Ses Filiales|January 1, 1973
[Separation of hexosaminidase isoenzymes in normal leukocytes, cultured fibroblasts and amniotic fluid cells: demonstration of 3 fractions]I Liebaers, E Vamos, I M Mandelbaum
Acta Clinica Belgica|January 1, 1974
Study of the beta-bexosyminidase separation by electrophoresis in homozygote and heterozygote Tay-Sachs cultured fibroblastsI Liebaers, E Vamos, I M Mandelbaum
Molecular and Cellular Endocrinology|March 20, 2002
Intracytoplasmic sperm injectionAndré Van Steirteghem, P Devroey, I Liebaers
Human Genetics|January 28, 1999
A mutation (IVS8+0.6kbdelTC) creating a new donor splice site activates a cryptic exon in an Alu-element in intron 8 of the human beta-glucuronidase geneR Vervoort, R Gitzelmann, W Lissens, et al.
Human Reproduction (Oxford, England)|September 28, 2002
Epigenetic risks related to assisted reproductive technologies: risk analysis and epigenetic inheritanceM De Rycke, I Liebaers, A Van Steirteghem
Advances in Experimental Medicine and Biology|January 1, 1976
Iduronate sulfatase determination for the diagnosis of the Hunter syndrome and the detection of the carrier stateE F Neufeld, I Liebaers, T W Lim
Biochemical and Biophysical Research Communications|May 31, 1982
Biochemical characterization of neonatal multiple sulfatase deficient (MSD) disorder cultured skin fibroblastsY Eto, T Tokoro, I Liebaers, et al.
The Journal of Pediatrics|March 1, 1977
Iduronate sulfatase in amniotic fluid: an aid in the prenatal diagnosis of the hunter syndromeI Liebaers, P Di Natale, E F Neufeld
Urologia Internationalis|August 8, 2001
DNA methylation analysis in immature testicular sperm cells at different developmental stagesM Manning, W Lissens, W Weidner, et al.
Human Genetics|March 1, 1992
Pyruvate dehydrogenase (PDH) deficiency caused by a 21-base pair insertion mutation in the E1 alpha subunitL De Meirleir, W Lissens, E Vamos, et al.
Pageof 22