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I Liebaers

Showing results (31-40 of 211) with videos related to

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Human Genetics|September 1, 1990
The deletion F508 is the major gene mutation in a representative Belgian cystic fibrosis populationM Bonduelle, W Lissens, A Malfroot, et al.
Journal of Inherited Metabolic Disease|January 1, 1981
Multiple sulphatase deficiency with early onsetE Vamos, I Liebaers, N Bousard, et al.
European Journal of Pediatrics|November 1, 1985
Neonatal hepatitis with obstructive jaundice in an SZ heterozygous alpha 1-antitrypsin-deficient boy and destructive lung disease in his SZ mother. A review of the literatureY Vandenplas, J Franckx, I Liebaers, et al.
European Journal of Pediatrics|August 17, 1978
Mucopolysaccharidosis II (Hunter disease) with corneal opacities. Report on two patients at the extremes of a wide clinical spectrumJ Spranger, M Cantz, J Gehler, et al.
Lancet (London, England)|July 20, 1991
Mild cystic fibrosis in child homozygous for G542 non-sense mutation in CF geneM Bonduelle, W Lissens, I Liebaers, et al.
Prenatal Diagnosis|September 1, 1993
Polymerase chain reaction analysis of the cystic fibrosis delta F508 mutation in human blastomeres following oocyte injection of a single sperm from a carrierJ Liu, W Lissens, P Devroey, et al.
Molecular Human Reproduction|May 10, 2005
DAZL expression in human oocytes, preimplantation embryos and embryonic stem cellsG Cauffman, H Van de Velde, I Liebaers, et al.
Fertility and Sterility|February 1, 1995
Amplification of exon 11 of the gene for the alpha-chain of beta-N-acetylhexosaminidase in single human blastomeresK Sermon, W Lissens, P Devroey, et al.
Nucleic Acids Research|August 25, 1990
Characterisation of a cDNA for porcine PDH-E1 alpha and comparison with the human cDNAK Sermon, L De Meirleir, I Elpers, et al.
Human Genetics|August 1, 1988
The role of fluorinated pyrimidine analogues in the induction of the in vitro expression of the fragile X chromosomeB Vandamme, I Liebaers, L Hens, et al.
Pageof 22

Showing results (31-40 of 211) with videos related to

Sort By:
Pageof 22
Human Genetics|September 1, 1990
The deletion F508 is the major gene mutation in a representative Belgian cystic fibrosis populationM Bonduelle, W Lissens, A Malfroot, et al.
Journal of Inherited Metabolic Disease|January 1, 1981
Multiple sulphatase deficiency with early onsetE Vamos, I Liebaers, N Bousard, et al.
European Journal of Pediatrics|November 1, 1985
Neonatal hepatitis with obstructive jaundice in an SZ heterozygous alpha 1-antitrypsin-deficient boy and destructive lung disease in his SZ mother. A review of the literatureY Vandenplas, J Franckx, I Liebaers, et al.
European Journal of Pediatrics|August 17, 1978
Mucopolysaccharidosis II (Hunter disease) with corneal opacities. Report on two patients at the extremes of a wide clinical spectrumJ Spranger, M Cantz, J Gehler, et al.
Lancet (London, England)|July 20, 1991
Mild cystic fibrosis in child homozygous for G542 non-sense mutation in CF geneM Bonduelle, W Lissens, I Liebaers, et al.
Prenatal Diagnosis|September 1, 1993
Polymerase chain reaction analysis of the cystic fibrosis delta F508 mutation in human blastomeres following oocyte injection of a single sperm from a carrierJ Liu, W Lissens, P Devroey, et al.
Molecular Human Reproduction|May 10, 2005
DAZL expression in human oocytes, preimplantation embryos and embryonic stem cellsG Cauffman, H Van de Velde, I Liebaers, et al.
Fertility and Sterility|February 1, 1995
Amplification of exon 11 of the gene for the alpha-chain of beta-N-acetylhexosaminidase in single human blastomeresK Sermon, W Lissens, P Devroey, et al.
Nucleic Acids Research|August 25, 1990
Characterisation of a cDNA for porcine PDH-E1 alpha and comparison with the human cDNAK Sermon, L De Meirleir, I Elpers, et al.
Human Genetics|August 1, 1988
The role of fluorinated pyrimidine analogues in the induction of the in vitro expression of the fragile X chromosomeB Vandamme, I Liebaers, L Hens, et al.
Pageof 22