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I Liebaers

Showing results (21-30 of 211) with videos related to

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Human Reproduction Update|July 9, 2002
Follow-up of children born after ICSIA Van Steirteghem, M Bonduelle, P Devroey, et al.
Lancet (London, England)|October 2, 1976
Genetic counselling for Hunter syndromeC J Epstein, S Yatziv, E Neufeld, et al.
Journal of Inherited Metabolic Disease|January 1, 1995
Importance of sequence analysis in NARP syndromeS Seneca, L De Meirleir, I Liebaers, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1997
How to counsel in osteopathia striata with cranial sclerosisK Keymolen, M Bonduelle, M De Maeseneer, et al.
Human Molecular Genetics|September 1, 1992
A serine to proline substitution (S1255P) in the second nucleotide binding fold of the cystic fibrosis geneW Lissens, M Bonduelle, A Malfroot, et al.
Journal of Medical Genetics|July 21, 2010
Methylation of the CpG sites in the myotonic dystrophy locus does not correlate with CTG expansion size or with the congenital form of the diseaseC Spits, S Seneca, P Hilven, et al.
Journal of Inherited Metabolic Disease|January 1, 1991
Pyruvate dehydrogenase deficiency due to a mutation of the E1 alpha subunitL J de Meirleir, W Lissens, E Vamos, et al.
Advances in Experimental Medicine and Biology|January 1, 1991
The prevalence of the deletion F508 in a Belgian cystic fibrosis populationW Lissens, M Bonduelle, A Malfroot, et al.
Pediatric Research|December 5, 2000
Analysis of exonic mutations leading to exon skipping in patients with pyruvate dehydrogenase E1 alpha deficiencyA K Cardozo, L De Meirleir, I Liebaers, et al.
Reproductive Biomedicine Online|December 4, 2010
Mutation analysis of three genes in patients with maturation arrest of spermatogenesis and couples with recurrent miscarriagesK Stouffs, D Vandermaelen, H Tournaye, et al.
Pageof 22

Showing results (21-30 of 211) with videos related to

Sort By:
Pageof 22
Human Reproduction Update|July 9, 2002
Follow-up of children born after ICSIA Van Steirteghem, M Bonduelle, P Devroey, et al.
Lancet (London, England)|October 2, 1976
Genetic counselling for Hunter syndromeC J Epstein, S Yatziv, E Neufeld, et al.
Journal of Inherited Metabolic Disease|January 1, 1995
Importance of sequence analysis in NARP syndromeS Seneca, L De Meirleir, I Liebaers, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1997
How to counsel in osteopathia striata with cranial sclerosisK Keymolen, M Bonduelle, M De Maeseneer, et al.
Human Molecular Genetics|September 1, 1992
A serine to proline substitution (S1255P) in the second nucleotide binding fold of the cystic fibrosis geneW Lissens, M Bonduelle, A Malfroot, et al.
Journal of Medical Genetics|July 21, 2010
Methylation of the CpG sites in the myotonic dystrophy locus does not correlate with CTG expansion size or with the congenital form of the diseaseC Spits, S Seneca, P Hilven, et al.
Journal of Inherited Metabolic Disease|January 1, 1991
Pyruvate dehydrogenase deficiency due to a mutation of the E1 alpha subunitL J de Meirleir, W Lissens, E Vamos, et al.
Advances in Experimental Medicine and Biology|January 1, 1991
The prevalence of the deletion F508 in a Belgian cystic fibrosis populationW Lissens, M Bonduelle, A Malfroot, et al.
Pediatric Research|December 5, 2000
Analysis of exonic mutations leading to exon skipping in patients with pyruvate dehydrogenase E1 alpha deficiencyA K Cardozo, L De Meirleir, I Liebaers, et al.
Reproductive Biomedicine Online|December 4, 2010
Mutation analysis of three genes in patients with maturation arrest of spermatogenesis and couples with recurrent miscarriagesK Stouffs, D Vandermaelen, H Tournaye, et al.
Pageof 22