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B Horsthemke

Showing results (31-40 of 176) with videos related to

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Clinical Genetics|October 1, 1985
A study of DNA polymorphisms around the human apolipoprotein AI gene in hyperlipidaemic and normal individualsA M Kessling, B Horsthemke, S E Humphries
Proceedings of the National Academy of Sciences of the United States of America|March 21, 1998
Identification of a silencing element in the human 15q11-q13 imprinting center by using transgenic DrosophilaF Lyko, K Buiting, B Horsthemke, et al.
Lancet (London, England)|March 14, 1992
Chromosomal aberrations defining uveal melanoma of poor prognosisG Prescher, N Bornfeld, B Horsthemke, et al.
American Journal of Medical Genetics|September 15, 1992
Deletion in one allele and a rare neutral DNA alteration in the other allele of the RB1 gene in a patient with bilateral retinoblastomaB Horsthemke, B Brandt, B Albrecht, et al.
Human Molecular Genetics|February 5, 1999
The chromosome 15 imprinting centre (IC) region has undergone multiple duplication events and contains an upstream exon of SNRPN that is deleted in all Angelman syndrome patients with an IC microdeletionC Färber, B Dittrich, K Buiting, et al.
Cytogenetics and Cell Genetics|January 1, 1988
No evidence for linkage between lipoprotein(a) (LPA) and esterase D (ESD)V Greger, E Gersdorf, G Utermann, et al.
Results and Problems in Cell Differentiation|May 26, 1999
The mechanisms of genomic imprintingB Horsthemke, A Surani, T James, et al.
Genes, Chromosomes & Cancer|April 1, 1992
Loss of chromosome 3 alleles and multiplication of chromosome 8 alleles in uveal melanomaB Horsthemke, G Prescher, N Bornfeld, et al.
Human Genetics|February 1, 1991
No evidence for sequences structurally related to the RB1 gene in the human genomeC Belka, V Greger, B Zabel, et al.
Human Molecular Genetics|December 1, 1993
Characterization of a methylation imprint in the Prader-Willi syndrome chromosome regionB Dittrich, K Buiting, S Gross, et al.
Pageof 18

Showing results (31-40 of 176) with videos related to

Sort By:
Pageof 18
Clinical Genetics|October 1, 1985
A study of DNA polymorphisms around the human apolipoprotein AI gene in hyperlipidaemic and normal individualsA M Kessling, B Horsthemke, S E Humphries
Proceedings of the National Academy of Sciences of the United States of America|March 21, 1998
Identification of a silencing element in the human 15q11-q13 imprinting center by using transgenic DrosophilaF Lyko, K Buiting, B Horsthemke, et al.
Lancet (London, England)|March 14, 1992
Chromosomal aberrations defining uveal melanoma of poor prognosisG Prescher, N Bornfeld, B Horsthemke, et al.
American Journal of Medical Genetics|September 15, 1992
Deletion in one allele and a rare neutral DNA alteration in the other allele of the RB1 gene in a patient with bilateral retinoblastomaB Horsthemke, B Brandt, B Albrecht, et al.
Human Molecular Genetics|February 5, 1999
The chromosome 15 imprinting centre (IC) region has undergone multiple duplication events and contains an upstream exon of SNRPN that is deleted in all Angelman syndrome patients with an IC microdeletionC Färber, B Dittrich, K Buiting, et al.
Cytogenetics and Cell Genetics|January 1, 1988
No evidence for linkage between lipoprotein(a) (LPA) and esterase D (ESD)V Greger, E Gersdorf, G Utermann, et al.
Results and Problems in Cell Differentiation|May 26, 1999
The mechanisms of genomic imprintingB Horsthemke, A Surani, T James, et al.
Genes, Chromosomes & Cancer|April 1, 1992
Loss of chromosome 3 alleles and multiplication of chromosome 8 alleles in uveal melanomaB Horsthemke, G Prescher, N Bornfeld, et al.
Human Genetics|February 1, 1991
No evidence for sequences structurally related to the RB1 gene in the human genomeC Belka, V Greger, B Zabel, et al.
Human Molecular Genetics|December 1, 1993
Characterization of a methylation imprint in the Prader-Willi syndrome chromosome regionB Dittrich, K Buiting, S Gross, et al.
Pageof 18