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K G Kupke

Showing results (1-10 of 14) with videos related to

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Human Genetics|January 1, 1990
The genetics of primary torsion dystoniaU Müller, K G Kupke
American Journal of Human Genetics|October 1, 1989
Parental origin of the extra chromosome in trisomy 18K G Kupke, U Müller
American Journal of Human Genetics|April 1, 1992
Dystonia-parkinsonism syndrome (XDP) locus: flanking markers in Xq12-q21.1K G Kupke, M B Graeber, U Müller
American Journal of Medical Genetics|February 1, 1991
Origin of the supernumerary X chromosome in a patient with fragile X and Klinefelter syndromeK G Kupke, A L Soreng, U Müller
Proceedings of the National Academy of Sciences of the United States of America|September 1, 1992
Delineation of the dystonia-parkinsonism syndrome locus in Xq13M B Graeber, K G Kupke, U Müller
Neurology|September 1, 1990
Assignment of the X-linked torsion dystonia gene to Xq21 by linkage analysisK G Kupke, L V Lee, U Müller
Journal of Medical Genetics|July 1, 1993
Second polar body incorporation into a blastomere results in 46,XX/69,XXX mixoploidyU Müller, J L Weber, P Berry, et al.
Scanning Electron Microscopy|January 1, 1985
Microprobe analysis in human pathologyD Baker, K G Kupke, P Ingram, et al.
Human Genetics|February 1, 1990
Maternal meiosis II nondisjunction in a case of 47,XXY testicular feminizationU Müller, N R Schneider, J F Marks, et al.
Human Mutation|February 12, 2000
Lys650Met substitution in the tyrosine kinase domain of the fibroblast growth factor receptor gene causes thanatophoric dysplasia Type I. Mutations in brief no. 199. OnlineH Kitoh, S G Brodie, K G Kupke, et al.
Pageof 2

Showing results (1-10 of 14) with videos related to

Sort By:
Pageof 2
Human Genetics|January 1, 1990
The genetics of primary torsion dystoniaU Müller, K G Kupke
American Journal of Human Genetics|October 1, 1989
Parental origin of the extra chromosome in trisomy 18K G Kupke, U Müller
American Journal of Human Genetics|April 1, 1992
Dystonia-parkinsonism syndrome (XDP) locus: flanking markers in Xq12-q21.1K G Kupke, M B Graeber, U Müller
American Journal of Medical Genetics|February 1, 1991
Origin of the supernumerary X chromosome in a patient with fragile X and Klinefelter syndromeK G Kupke, A L Soreng, U Müller
Proceedings of the National Academy of Sciences of the United States of America|September 1, 1992
Delineation of the dystonia-parkinsonism syndrome locus in Xq13M B Graeber, K G Kupke, U Müller
Neurology|September 1, 1990
Assignment of the X-linked torsion dystonia gene to Xq21 by linkage analysisK G Kupke, L V Lee, U Müller
Journal of Medical Genetics|July 1, 1993
Second polar body incorporation into a blastomere results in 46,XX/69,XXX mixoploidyU Müller, J L Weber, P Berry, et al.
Scanning Electron Microscopy|January 1, 1985
Microprobe analysis in human pathologyD Baker, K G Kupke, P Ingram, et al.
Human Genetics|February 1, 1990
Maternal meiosis II nondisjunction in a case of 47,XXY testicular feminizationU Müller, N R Schneider, J F Marks, et al.
Human Mutation|February 12, 2000
Lys650Met substitution in the tyrosine kinase domain of the fibroblast growth factor receptor gene causes thanatophoric dysplasia Type I. Mutations in brief no. 199. OnlineH Kitoh, S G Brodie, K G Kupke, et al.
Pageof 2