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Showing results (111-120 of 211) with videos related to

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Prenatal Diagnosis|November 14, 1997
Clinical application of preimplantation diagnosis for myotonic dystrophyK Sermon, W Lissens, H Joris, et al.
Journal of Medical Genetics|May 1, 1993
Mild pulmonary, but severe hepatic disease in a cystic fibrosis patient homozygous for a frameshift mutation in the regulatory domain of the CFTRW Lissens, S Desmyttere, M Bonduelle, et al.
Human Mutation|January 1, 1995
Identification of two novel mutations in the cystic fibrosis gene: 1898+3A-->C and 2711delTB Mercier, W Lissens, M P Audrézet, et al.
Acta Neuropathologica|January 1, 1993
Neuropathological findings of a patient with pyruvate dehydrogenase E1 alpha deficiency presenting as a cerebral lactic acidosisA Michotte, L De Meirleir, W Lissens, et al.
Human Reproduction (Oxford, England)|December 1, 1996
Obstetric outcome of 904 pregnancies after intracytoplasmic sperm injectionA Wisanto, M Bonduelle, M Camus, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1991
Lysosomal storage diseases presenting as transient or persistent hydrops fetalisM Bonduelle, W Lissens, A Goossens, et al.
Human Reproduction (Oxford, England)|August 1, 1988
Oocyte donation in patients without ovarian functionP Devroey, A Wisanto, M Camus, et al.
Annales De Biologie Clinique|January 1, 1987
First trimester prenatal diagnosis of lysosomal storage disease. Study of alpha-L-fucosidase isoenzyme patterns in fetal and maternal tissueW Lissens, T Bril, M Vercammen, et al.
Reproductive Biomedicine Online|April 13, 2005
HLA-matched embryos selected for siblings requiring haematopoietic stem cell transplantation: a psychological perspectiveP Baetens, H Van de Velde, M Camus, et al.
Prenatal Diagnosis|August 1, 1991
Beta-glucuronidase activity in mouse oocytes, mouse preimplantation embryos, and human gametesM Van Blerk, W Lissens, M Nijs, et al.
Pageof 22

Showing results (111-120 of 211) with videos related to

Sort By:
Pageof 22
Prenatal Diagnosis|November 14, 1997
Clinical application of preimplantation diagnosis for myotonic dystrophyK Sermon, W Lissens, H Joris, et al.
Journal of Medical Genetics|May 1, 1993
Mild pulmonary, but severe hepatic disease in a cystic fibrosis patient homozygous for a frameshift mutation in the regulatory domain of the CFTRW Lissens, S Desmyttere, M Bonduelle, et al.
Human Mutation|January 1, 1995
Identification of two novel mutations in the cystic fibrosis gene: 1898+3A-->C and 2711delTB Mercier, W Lissens, M P Audrézet, et al.
Acta Neuropathologica|January 1, 1993
Neuropathological findings of a patient with pyruvate dehydrogenase E1 alpha deficiency presenting as a cerebral lactic acidosisA Michotte, L De Meirleir, W Lissens, et al.
Human Reproduction (Oxford, England)|December 1, 1996
Obstetric outcome of 904 pregnancies after intracytoplasmic sperm injectionA Wisanto, M Bonduelle, M Camus, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1991
Lysosomal storage diseases presenting as transient or persistent hydrops fetalisM Bonduelle, W Lissens, A Goossens, et al.
Human Reproduction (Oxford, England)|August 1, 1988
Oocyte donation in patients without ovarian functionP Devroey, A Wisanto, M Camus, et al.
Annales De Biologie Clinique|January 1, 1987
First trimester prenatal diagnosis of lysosomal storage disease. Study of alpha-L-fucosidase isoenzyme patterns in fetal and maternal tissueW Lissens, T Bril, M Vercammen, et al.
Reproductive Biomedicine Online|April 13, 2005
HLA-matched embryos selected for siblings requiring haematopoietic stem cell transplantation: a psychological perspectiveP Baetens, H Van de Velde, M Camus, et al.
Prenatal Diagnosis|August 1, 1991
Beta-glucuronidase activity in mouse oocytes, mouse preimplantation embryos, and human gametesM Van Blerk, W Lissens, M Nijs, et al.
Pageof 22