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K Buiting

Showing results (21-30 of 65) with videos related to

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Human Molecular Genetics|December 1, 2001
The IC-SNURF-SNRPN transcript serves as a host for multiple small nucleolar RNA species and as an antisense RNA for UBE3AM Runte, A Hüttenhofer, S Gross, et al.
Klinische Padiatrie|June 2, 2010
Slow progression of a small Wilms' tumorT Simon, M Feldkötter, K Buiting, et al.
Journal of Medical Genetics|December 14, 2004
Recurrent deletion of a region containing exon 24 of the RB1 gene caused by non-homologous recombination between a LINE-1HS and MER21B elementP Albrecht, J Bode, K Buiting, et al.
Human Molecular Genetics|March 1, 1997
Imprinted segments in the human genome: different DNA methylation patterns in the Prader-Willi/Angelman syndrome region as determined by the genomic sequencing methodM Zeschnigk, B Schmitz, B Dittrich, et al.
American Journal of Human Genetics|April 3, 2001
Disruption of the bipartite imprinting center in a family with Angelman syndromeK Buiting, A Barnicoat, C Lich, et al.
Clinical Genetics|April 19, 2003
Molecular characterization of a unique de novo 15q deletion associated with Prader-Willi syndrome and central visual impairmentC Windpassinger, E Petek, K Wagner, et al.
Cytogenetics and Cell Genetics|September 8, 1998
Expressed copies of the MN7 (D15F37) gene family map close to the common deletion breakpoints in the Prader-Willi/Angelman syndromesK Buiting, S Gross, Y Ji, et al.
Human Mutation|January 1, 1996
A familial deletion in the Prader-Willi syndrome region including the imprinting control regionS Schuffenhauer, T Buchholz, S Stengel-Rutkowski, et al.
Clinical Genetics|January 4, 2012
Deletion of the paternal allele of the imprinted MEST/PEG1 region in a patient with Silver-Russell syndrome featuresT Eggermann, S Spengler, M Begemann, et al.
Human Genetics|April 3, 2001
Marked differences in unilateral isolated retinoblastomas from young and older children studied by comparative genomic hybridizationS Herzog, D R Lohmann, K Buiting, et al.
Pageof 7

Showing results (21-30 of 65) with videos related to

Sort By:
Pageof 7
Human Molecular Genetics|December 1, 2001
The IC-SNURF-SNRPN transcript serves as a host for multiple small nucleolar RNA species and as an antisense RNA for UBE3AM Runte, A Hüttenhofer, S Gross, et al.
Klinische Padiatrie|June 2, 2010
Slow progression of a small Wilms' tumorT Simon, M Feldkötter, K Buiting, et al.
Journal of Medical Genetics|December 14, 2004
Recurrent deletion of a region containing exon 24 of the RB1 gene caused by non-homologous recombination between a LINE-1HS and MER21B elementP Albrecht, J Bode, K Buiting, et al.
Human Molecular Genetics|March 1, 1997
Imprinted segments in the human genome: different DNA methylation patterns in the Prader-Willi/Angelman syndrome region as determined by the genomic sequencing methodM Zeschnigk, B Schmitz, B Dittrich, et al.
American Journal of Human Genetics|April 3, 2001
Disruption of the bipartite imprinting center in a family with Angelman syndromeK Buiting, A Barnicoat, C Lich, et al.
Clinical Genetics|April 19, 2003
Molecular characterization of a unique de novo 15q deletion associated with Prader-Willi syndrome and central visual impairmentC Windpassinger, E Petek, K Wagner, et al.
Cytogenetics and Cell Genetics|September 8, 1998
Expressed copies of the MN7 (D15F37) gene family map close to the common deletion breakpoints in the Prader-Willi/Angelman syndromesK Buiting, S Gross, Y Ji, et al.
Human Mutation|January 1, 1996
A familial deletion in the Prader-Willi syndrome region including the imprinting control regionS Schuffenhauer, T Buchholz, S Stengel-Rutkowski, et al.
Clinical Genetics|January 4, 2012
Deletion of the paternal allele of the imprinted MEST/PEG1 region in a patient with Silver-Russell syndrome featuresT Eggermann, S Spengler, M Begemann, et al.
Human Genetics|April 3, 2001
Marked differences in unilateral isolated retinoblastomas from young and older children studied by comparative genomic hybridizationS Herzog, D R Lohmann, K Buiting, et al.
Pageof 7