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B Dittrich

Showing results (41-50 of 55) with videos related to

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Biotechnology and Bioengineering|June 1, 2006
Fed-batch mode in shake flasks by slow-release techniqueM Jeude, B Dittrich, H Niederschulte, et al.
Human Molecular Genetics|June 1, 1994
Detection of aberrant DNA methylation in unique Prader-Willi syndrome patients and its diagnostic implicationsK Buiting, B Dittrich, W P Robinson, et al.
Nature Genetics|April 1, 1995
Inherited microdeletions in the Angelman and Prader-Willi syndromes define an imprinting centre on human chromosome 15K Buiting, S Saitoh, S Gross, et al.
American Journal of Human Genetics|July 1, 1997
Different mechanisms and recurrence risks of imprinting defects in Angelman syndromeJ Bürger, K Buiting, B Dittrich, et al.
Human Genetics|November 1, 1992
Molecular diagnosis of the Prader-Willi and Angelman syndromes by detection of parent-of-origin specific DNA methylation in 15q11-13B Dittrich, W P Robinson, H Knoblauch, et al.
American Journal of Human Genetics|May 1, 1994
Imprinting mutations suggested by abnormal DNA methylation patterns in familial Angelman and Prader-Willi syndromesA Reis, B Dittrich, V Greger, et al.
Acta Crystallographica Section B, Structural Science, Crystal Engineering and Materials|October 10, 2018
Azulene revisited: solid-state structure, invariom modeling and lattice-energy minimization of a classical example of disorderB Dittrich, F P A Fabbiani, J Henn, et al.
Human Molecular Genetics|December 1, 1993
Molecular definition of the Prader-Willi syndrome chromosome region and orientation of the SNRPN geneK Buiting, B Dittrich, S Gross, et al.
Human Molecular Genetics|September 1, 1992
Molecular dissection of the Prader-Willi/Angelman syndrome region (15q11-13) by YAC cloning and FISH analysisA Kuwano, A Mutirangura, B Dittrich, et al.
Nature Genetics|October 1, 1996
Imprint switching on human chromosome 15 may involve alternative transcripts of the SNRPN geneB Dittrich, K Buiting, B Korn, et al.
Pageof 6

Showing results (41-50 of 55) with videos related to

Sort By:
Pageof 6
Biotechnology and Bioengineering|June 1, 2006
Fed-batch mode in shake flasks by slow-release techniqueM Jeude, B Dittrich, H Niederschulte, et al.
Human Molecular Genetics|June 1, 1994
Detection of aberrant DNA methylation in unique Prader-Willi syndrome patients and its diagnostic implicationsK Buiting, B Dittrich, W P Robinson, et al.
Nature Genetics|April 1, 1995
Inherited microdeletions in the Angelman and Prader-Willi syndromes define an imprinting centre on human chromosome 15K Buiting, S Saitoh, S Gross, et al.
American Journal of Human Genetics|July 1, 1997
Different mechanisms and recurrence risks of imprinting defects in Angelman syndromeJ Bürger, K Buiting, B Dittrich, et al.
Human Genetics|November 1, 1992
Molecular diagnosis of the Prader-Willi and Angelman syndromes by detection of parent-of-origin specific DNA methylation in 15q11-13B Dittrich, W P Robinson, H Knoblauch, et al.
American Journal of Human Genetics|May 1, 1994
Imprinting mutations suggested by abnormal DNA methylation patterns in familial Angelman and Prader-Willi syndromesA Reis, B Dittrich, V Greger, et al.
Acta Crystallographica Section B, Structural Science, Crystal Engineering and Materials|October 10, 2018
Azulene revisited: solid-state structure, invariom modeling and lattice-energy minimization of a classical example of disorderB Dittrich, F P A Fabbiani, J Henn, et al.
Human Molecular Genetics|December 1, 1993
Molecular definition of the Prader-Willi syndrome chromosome region and orientation of the SNRPN geneK Buiting, B Dittrich, S Gross, et al.
Human Molecular Genetics|September 1, 1992
Molecular dissection of the Prader-Willi/Angelman syndrome region (15q11-13) by YAC cloning and FISH analysisA Kuwano, A Mutirangura, B Dittrich, et al.
Nature Genetics|October 1, 1996
Imprint switching on human chromosome 15 may involve alternative transcripts of the SNRPN geneB Dittrich, K Buiting, B Korn, et al.
Pageof 6