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N Van Roy

Showing results (21-30 of 90) with videos related to

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Clinical Genetics|September 1, 1992
Putative monosomy 21 in two patients: clinical findings and investigation using fluorescence in situ hybridizationD L Viljoen, F Speleman, R Smart, et al.
Genomics|April 7, 1999
Closing in on the BPES gene on 3q23: mapping of a de Novo reciprocal translocation t(3;4)(q23;p15.2) breakpoint within a 45-kb cosmid and mapping of three candidate genes, RBP1, RBP2, and beta'-COP, distal to the breakpointE De Baere, N Van Roy, F Speleman, et al.
Cytogenetics and Cell Genetics|March 11, 1999
Assignment of the cellular retinol-binding protein 2 gene (RBP2) to human chromosome band 3q23 by in situ hybridizationE De Baere, F Speleman, N Van Roy, et al.
Cytogenetics and Cell Genetics|January 1, 1995
Assignment of the human beta-catenin gene (CTNNB1) to 3p22-->p21.3 by fluorescence in situ hybridizationJ van Hengel, F Nollet, G Berx, et al.
European Journal of Cancer (Oxford, England : 1990)|April 28, 2004
Molecular analysis of the putative tumour-suppressor gene EXTL1 in neuroblastoma patients and cell linesD Mathysen, N Van Roy, W Van Hul, et al.
Genes, Chromosomes & Cancer|June 1, 1994
1;17 translocations and other chromosome 17 rearrangements in human primary neuroblastoma tumors and cell linesN Van Roy, G Laureys, N C Cheng, et al.
Clinical Genetics|September 1, 1993
Molecular cytogenetic analysis of a familial pericentric inversion of chromosome 12F Speleman, N Van Roy, E De Vos, et al.
Oncogene|January 19, 1995
Deletion mapping in neuroblastoma cell lines suggests two distinct tumor suppressor genes in the 1p35-36 region, only one of which is associated with N-myc amplificationN C Cheng, N Van Roy, A Chan, et al.
European Journal of Cancer (Oxford, England : 1990)|January 1, 1995
Characterisation of the chromosome breakpoints in a patient with a constitutional translocation t(1;17)(p36.31-p36.13;q11.2-q12) and neuroblastomaG Laureys, R Versteeg, F Speleman, et al.
Human Molecular Genetics|December 1, 1994
A multimegabase cluster of snRNA and tRNA genes on chromosome 1p36 harbours an adenovirus/SV40 hybrid virus integration siteP van der Drift, A Chan, N van Roy, et al.
Pageof 9

Showing results (21-30 of 90) with videos related to

Sort By:
Pageof 9
Clinical Genetics|September 1, 1992
Putative monosomy 21 in two patients: clinical findings and investigation using fluorescence in situ hybridizationD L Viljoen, F Speleman, R Smart, et al.
Genomics|April 7, 1999
Closing in on the BPES gene on 3q23: mapping of a de Novo reciprocal translocation t(3;4)(q23;p15.2) breakpoint within a 45-kb cosmid and mapping of three candidate genes, RBP1, RBP2, and beta'-COP, distal to the breakpointE De Baere, N Van Roy, F Speleman, et al.
Cytogenetics and Cell Genetics|March 11, 1999
Assignment of the cellular retinol-binding protein 2 gene (RBP2) to human chromosome band 3q23 by in situ hybridizationE De Baere, F Speleman, N Van Roy, et al.
Cytogenetics and Cell Genetics|January 1, 1995
Assignment of the human beta-catenin gene (CTNNB1) to 3p22-->p21.3 by fluorescence in situ hybridizationJ van Hengel, F Nollet, G Berx, et al.
European Journal of Cancer (Oxford, England : 1990)|April 28, 2004
Molecular analysis of the putative tumour-suppressor gene EXTL1 in neuroblastoma patients and cell linesD Mathysen, N Van Roy, W Van Hul, et al.
Genes, Chromosomes & Cancer|June 1, 1994
1;17 translocations and other chromosome 17 rearrangements in human primary neuroblastoma tumors and cell linesN Van Roy, G Laureys, N C Cheng, et al.
Clinical Genetics|September 1, 1993
Molecular cytogenetic analysis of a familial pericentric inversion of chromosome 12F Speleman, N Van Roy, E De Vos, et al.
Oncogene|January 19, 1995
Deletion mapping in neuroblastoma cell lines suggests two distinct tumor suppressor genes in the 1p35-36 region, only one of which is associated with N-myc amplificationN C Cheng, N Van Roy, A Chan, et al.
European Journal of Cancer (Oxford, England : 1990)|January 1, 1995
Characterisation of the chromosome breakpoints in a patient with a constitutional translocation t(1;17)(p36.31-p36.13;q11.2-q12) and neuroblastomaG Laureys, R Versteeg, F Speleman, et al.
Human Molecular Genetics|December 1, 1994
A multimegabase cluster of snRNA and tRNA genes on chromosome 1p36 harbours an adenovirus/SV40 hybrid virus integration siteP van der Drift, A Chan, N van Roy, et al.
Pageof 9