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I Liebaers

Showing results (121-130 of 211) with videos related to

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Journal of Inherited Metabolic Disease|January 1, 1989
Prenatal diagnosis of cystic fibrosis using closely linked DNA probesW Lissens, M Vercammen, W Foulon, et al.
Human Reproduction (Oxford, England)|July 15, 1998
A follow-up study of children born after intracytoplasmic sperm injection (ICSI) with epididymal and testicular spermatozoa and after replacement of cryopreserved embryos obtained after ICSIM Bonduelle, A Wilikens, A Buysse, et al.
Human Genetics|April 1, 1997
Molecular analysis of the beta-glucuronidase gene: novel mutations in mucopolysaccharidosis type VII and heterogeneity of the polyadenylation regionR Vervoort, N R Buist, W J Kleijer, et al.
Prenatal Diagnosis|February 8, 2000
Preimplantation diagnosis for fragile X syndrome based on the detection of the non-expanded paternal and maternal CGGK Sermon, S Seneca, A Vanderfaeillie, et al.
Human Reproduction (Oxford, England)|August 6, 2009
Cumulative reproductive outcome after preimplantation genetic diagnosis: a report on 1498 couplesW Verpoest, P Haentjens, M De Rycke, et al.
Journal of Medical Genetics|December 1, 1998
Pitfalls in the diagnosis of mtDNA mutationsS Seneca, W Lissens, I Liebaers, et al.
Molecular Human Reproduction|March 2, 1999
Molecular analysis of the cystic fibrosis gene reveals a high frequency of the intron 8 splice variant 5T in Egyptian males with congenital bilateral absence of the vas deferensW Lissens, K Z Mahmoud, E El-Gindi, et al.
Human Reproduction (Oxford, England)|December 1, 2000
ESHRE preimplantation genetic diagnosis (PGD) consortium: data collection II (May 2000)J Geraedts, A Handyside, J Harper, et al.
Acta Paediatrica Belgica|April 1, 1976
Antenatal diagnosis of congenital diseases through cultured amniotic cells: results of 149 amniocentesesE Vamos-Hurwitz, P Petit, I Liebaers, et al.
Human Mutation|April 19, 2006
Optimization and evaluation of single-cell whole-genome multiple displacement amplificationC Spits, C Le Caignec, M De Rycke, et al.
Pageof 22

Showing results (121-130 of 211) with videos related to

Sort By:
Pageof 22
Journal of Inherited Metabolic Disease|January 1, 1989
Prenatal diagnosis of cystic fibrosis using closely linked DNA probesW Lissens, M Vercammen, W Foulon, et al.
Human Reproduction (Oxford, England)|July 15, 1998
A follow-up study of children born after intracytoplasmic sperm injection (ICSI) with epididymal and testicular spermatozoa and after replacement of cryopreserved embryos obtained after ICSIM Bonduelle, A Wilikens, A Buysse, et al.
Human Genetics|April 1, 1997
Molecular analysis of the beta-glucuronidase gene: novel mutations in mucopolysaccharidosis type VII and heterogeneity of the polyadenylation regionR Vervoort, N R Buist, W J Kleijer, et al.
Prenatal Diagnosis|February 8, 2000
Preimplantation diagnosis for fragile X syndrome based on the detection of the non-expanded paternal and maternal CGGK Sermon, S Seneca, A Vanderfaeillie, et al.
Human Reproduction (Oxford, England)|August 6, 2009
Cumulative reproductive outcome after preimplantation genetic diagnosis: a report on 1498 couplesW Verpoest, P Haentjens, M De Rycke, et al.
Journal of Medical Genetics|December 1, 1998
Pitfalls in the diagnosis of mtDNA mutationsS Seneca, W Lissens, I Liebaers, et al.
Molecular Human Reproduction|March 2, 1999
Molecular analysis of the cystic fibrosis gene reveals a high frequency of the intron 8 splice variant 5T in Egyptian males with congenital bilateral absence of the vas deferensW Lissens, K Z Mahmoud, E El-Gindi, et al.
Human Reproduction (Oxford, England)|December 1, 2000
ESHRE preimplantation genetic diagnosis (PGD) consortium: data collection II (May 2000)J Geraedts, A Handyside, J Harper, et al.
Acta Paediatrica Belgica|April 1, 1976
Antenatal diagnosis of congenital diseases through cultured amniotic cells: results of 149 amniocentesesE Vamos-Hurwitz, P Petit, I Liebaers, et al.
Human Mutation|April 19, 2006
Optimization and evaluation of single-cell whole-genome multiple displacement amplificationC Spits, C Le Caignec, M De Rycke, et al.
Pageof 22