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B Horsthemke

Showing results (51-60 of 176) with videos related to

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Nature|March 23, 1989
Cloning defined regions of the human genome by microdissection of banded chromosomes and enzymatic amplificationH J Lüdecke, G Senger, U Claussen, et al.
Human Genetics|May 1, 1990
Microdissection of banded human chromosomesG Senger, H J Lüdecke, B Horsthemke, et al.
Human Genetics|May 1, 1990
Construction and characterization of band-specific DNA librariesH J Lüdecke, G Senger, U Claussen, et al.
Cytogenetics and Cell Genetics|January 21, 2000
The human gene for the poly(A)-specific ribonuclease (PARN) maps to 16p13 and has a truncated copy in the Prader-Willi/Angelman syndrome region on 15q11-->q13K Buiting, C Körner, B Ulrich, et al.
Human Genetics|January 27, 2000
A 5-kb imprinting center deletion in a family with Angelman syndrome reduces the shortest region of deletion overlap to 880 bpK Buiting, C Lich, S Cottrell, et al.
Genomics|April 28, 2000
Identification of a testis-specific gene (C15orf2) in the Prader-Willi syndrome region on chromosome 15C Färber, S Gross, J Neesen, et al.
European Journal of Human Genetics : EJHG|March 1, 1997
A single-tube PCR test for the diagnosis of Angelman and Prader-Willi syndrome based on allelic methylation differences at the SNRPN locusM Zeschnigk, C Lich, K Buiting, et al.
Cytogenetics and Cell Genetics|January 1, 1997
The murine Ext1 gene shows a high level of sequence similarity with its human homologue and is part of a conserved linkage group on chromosome 15D R Lohmann, K Buiting, H J Lüdecke, et al.
International Journal of Andrology|November 3, 2009
Idiopathic male infertility is strongly associated with aberrant methylation of MEST and IGF2/H19 ICR1A Poplinski, F Tüttelmann, D Kanber, et al.
Human Genetics|September 1, 1989
Epigenetic changes may contribute to the formation and spontaneous regression of retinoblastomaV Greger, E Passarge, W Höpping, et al.
Pageof 18

Showing results (51-60 of 176) with videos related to

Sort By:
Pageof 18
Nature|March 23, 1989
Cloning defined regions of the human genome by microdissection of banded chromosomes and enzymatic amplificationH J Lüdecke, G Senger, U Claussen, et al.
Human Genetics|May 1, 1990
Microdissection of banded human chromosomesG Senger, H J Lüdecke, B Horsthemke, et al.
Human Genetics|May 1, 1990
Construction and characterization of band-specific DNA librariesH J Lüdecke, G Senger, U Claussen, et al.
Cytogenetics and Cell Genetics|January 21, 2000
The human gene for the poly(A)-specific ribonuclease (PARN) maps to 16p13 and has a truncated copy in the Prader-Willi/Angelman syndrome region on 15q11-->q13K Buiting, C Körner, B Ulrich, et al.
Human Genetics|January 27, 2000
A 5-kb imprinting center deletion in a family with Angelman syndrome reduces the shortest region of deletion overlap to 880 bpK Buiting, C Lich, S Cottrell, et al.
Genomics|April 28, 2000
Identification of a testis-specific gene (C15orf2) in the Prader-Willi syndrome region on chromosome 15C Färber, S Gross, J Neesen, et al.
European Journal of Human Genetics : EJHG|March 1, 1997
A single-tube PCR test for the diagnosis of Angelman and Prader-Willi syndrome based on allelic methylation differences at the SNRPN locusM Zeschnigk, C Lich, K Buiting, et al.
Cytogenetics and Cell Genetics|January 1, 1997
The murine Ext1 gene shows a high level of sequence similarity with its human homologue and is part of a conserved linkage group on chromosome 15D R Lohmann, K Buiting, H J Lüdecke, et al.
International Journal of Andrology|November 3, 2009
Idiopathic male infertility is strongly associated with aberrant methylation of MEST and IGF2/H19 ICR1A Poplinski, F Tüttelmann, D Kanber, et al.
Human Genetics|September 1, 1989
Epigenetic changes may contribute to the formation and spontaneous regression of retinoblastomaV Greger, E Passarge, W Höpping, et al.
Pageof 18