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W Schempp

Showing results (51-60 of 97) with videos related to

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Clinical Genetics|June 1, 1993
A retrospective CISS hybridization analysis of a case with de novo translocation t(18;22) resulting in an 18p- syndromeI Voiculescu, R Toder, E Back, et al.
Heredity|November 3, 2011
Centromere repositioning in mammalsM Rocchi, N Archidiacono, W Schempp, et al.
Human Genetics|January 1, 1981
Characterization of a new aberration of the human Y chromosome by banding methods and DNA restriction endonuclease analysisM Schmid, H Gall, W Schempp, et al.
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|May 2, 2001
Loss of the Y chromosomal PAR2-region in four familial cases of satellited Y chromosomes (Yqs)H Kühl, S Röttger, H Heilbronner, et al.
Human Genetics|October 1, 1987
A Y/5 translocation in a 45,X male with cri du chat syndromeB Weber, W Schempp, U Orth, et al.
Genes, Chromosomes & Cancer|July 1, 1990
Chromosome abnormalities in multiple meningiomas of a childB Wullich, L Mayfrank, K Schwechheimer, et al.
Cytogenetic and Genome Research|August 6, 2003
The Azoospermia region AZFa: an evolutionar y viewR Wimmer, S Kirsch, A Weber, et al.
Human Genetics|July 1, 1987
Trisomy 22 in a newborn with multiple malformationsI Voiculescu, E Back, A M Duncan, et al.
Human Genetics|January 1, 1985
A 45,X male with evidence of a translocation of Y euchromatin onto chromosome 15W Schempp, B Weber, A Serra, et al.
Human Genetics|January 1, 1984
Satellited Y chromosomes: structure, origin, and clinical significanceM Schmid, T Haaf, E Solleder, et al.
Pageof 10

Showing results (51-60 of 97) with videos related to

Sort By:
Pageof 10
Clinical Genetics|June 1, 1993
A retrospective CISS hybridization analysis of a case with de novo translocation t(18;22) resulting in an 18p- syndromeI Voiculescu, R Toder, E Back, et al.
Heredity|November 3, 2011
Centromere repositioning in mammalsM Rocchi, N Archidiacono, W Schempp, et al.
Human Genetics|January 1, 1981
Characterization of a new aberration of the human Y chromosome by banding methods and DNA restriction endonuclease analysisM Schmid, H Gall, W Schempp, et al.
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|May 2, 2001
Loss of the Y chromosomal PAR2-region in four familial cases of satellited Y chromosomes (Yqs)H Kühl, S Röttger, H Heilbronner, et al.
Human Genetics|October 1, 1987
A Y/5 translocation in a 45,X male with cri du chat syndromeB Weber, W Schempp, U Orth, et al.
Genes, Chromosomes & Cancer|July 1, 1990
Chromosome abnormalities in multiple meningiomas of a childB Wullich, L Mayfrank, K Schwechheimer, et al.
Cytogenetic and Genome Research|August 6, 2003
The Azoospermia region AZFa: an evolutionar y viewR Wimmer, S Kirsch, A Weber, et al.
Human Genetics|July 1, 1987
Trisomy 22 in a newborn with multiple malformationsI Voiculescu, E Back, A M Duncan, et al.
Human Genetics|January 1, 1985
A 45,X male with evidence of a translocation of Y euchromatin onto chromosome 15W Schempp, B Weber, A Serra, et al.
Human Genetics|January 1, 1984
Satellited Y chromosomes: structure, origin, and clinical significanceM Schmid, T Haaf, E Solleder, et al.
Pageof 10