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M Mannens

Showing results (41-50 of 172) with videos related to

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Cytogenetics and Cell Genetics|January 1, 1993
Reassessment of breakpoints in chromosome 11p15I Henry, V van Heyningen, A Puech, et al.
European Journal of Human Genetics : EJHG|January 1, 1993
Somatic mosaicism for partial paternal isodisomy in Wiedemann-Beckwith syndrome: a post-fertilization eventI Henry, A Puech, A Riesewijk, et al.
Human Genetics|December 1, 1988
Molecular nature of genetic changes resulting in loss of heterozygosity of chromosome 11 in Wilms' tumoursM Mannens, R M Slater, C Heyting, et al.
Genes, Chromosomes & Cancer|May 1, 1993
Pericentric intrachromosomal insertion responsible for recurrence of del(11)(p13p14) in a familyI Henry, J Hoovers, F Barichard, et al.
Clinical and Experimental Immunology|November 1, 1995
Fulminant meningococcal septic shock in a boy with combined inherited properdin and protein C deficiencyC A Fijen, B H Derkx, E J Kuijper, et al.
Cytogenetics and Cell Genetics|January 1, 1989
Assignment of the gene coding for human peroxisomal 3-oxoacyl-CoA thiolase (ACAA) to chromosome region 3p22----p23A Bout, J M Hoovers, E Bakker, et al.
Circulation|September 24, 1999
Homozygous premature truncation of the HERG protein : the human HERG knockoutT Hoorntje, M Alders, P van Tintelen, et al.
Genetic Testing|June 24, 2006
Molecular genetic testing for familial hypercholesterolemia in the Netherlands: a stepwise screening strategy enhances the mutation detection rateM P Lombardi, E J W Redeker, D H M van Gent, et al.
Epigenomics|March 2, 2022
Prenatal NeuN+ neurons of Down syndrome display aberrant integrative DNA methylation and gene expression profilesPeter Henneman, Adri N Mul, Andrew Yf Li Yim, et al.
Journal of Medical Genetics|October 21, 2005
Genotype-phenotype correlations of 39 patients with Cornelia De Lange syndrome: the Dutch experienceZ A Bhuiyan, M Klein, P Hammond, et al.
Pageof 18

Showing results (41-50 of 172) with videos related to

Sort By:
Pageof 18
Cytogenetics and Cell Genetics|January 1, 1993
Reassessment of breakpoints in chromosome 11p15I Henry, V van Heyningen, A Puech, et al.
European Journal of Human Genetics : EJHG|January 1, 1993
Somatic mosaicism for partial paternal isodisomy in Wiedemann-Beckwith syndrome: a post-fertilization eventI Henry, A Puech, A Riesewijk, et al.
Human Genetics|December 1, 1988
Molecular nature of genetic changes resulting in loss of heterozygosity of chromosome 11 in Wilms' tumoursM Mannens, R M Slater, C Heyting, et al.
Genes, Chromosomes & Cancer|May 1, 1993
Pericentric intrachromosomal insertion responsible for recurrence of del(11)(p13p14) in a familyI Henry, J Hoovers, F Barichard, et al.
Clinical and Experimental Immunology|November 1, 1995
Fulminant meningococcal septic shock in a boy with combined inherited properdin and protein C deficiencyC A Fijen, B H Derkx, E J Kuijper, et al.
Cytogenetics and Cell Genetics|January 1, 1989
Assignment of the gene coding for human peroxisomal 3-oxoacyl-CoA thiolase (ACAA) to chromosome region 3p22----p23A Bout, J M Hoovers, E Bakker, et al.
Circulation|September 24, 1999
Homozygous premature truncation of the HERG protein : the human HERG knockoutT Hoorntje, M Alders, P van Tintelen, et al.
Genetic Testing|June 24, 2006
Molecular genetic testing for familial hypercholesterolemia in the Netherlands: a stepwise screening strategy enhances the mutation detection rateM P Lombardi, E J W Redeker, D H M van Gent, et al.
Epigenomics|March 2, 2022
Prenatal NeuN+ neurons of Down syndrome display aberrant integrative DNA methylation and gene expression profilesPeter Henneman, Adri N Mul, Andrew Yf Li Yim, et al.
Journal of Medical Genetics|October 21, 2005
Genotype-phenotype correlations of 39 patients with Cornelia De Lange syndrome: the Dutch experienceZ A Bhuiyan, M Klein, P Hammond, et al.
Pageof 18