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Cytogenetic and Genome Research
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March 9, 2004
Multitude multicolor chromosome banding (mMCB) - a comprehensive one-step multicolor FISH banding method
A Weise, A Heller, H Starke, et al.
Cytogenetic and Genome Research
|
November 20, 2002
Multicolor chromosome banding (MCB) with YAC/BAC-based probes and region-specific microdissection DNA libraries
T Liehr, A Weise, A Heller, et al.
Cytogenetic and Genome Research
|
September 7, 2006
Supernumerary marker chromosome 5 diagnosed by M-FISH in a child with congenital heart defect and unusual face
C Sarri, Y Gyftodimou, M Grigoriadou, et al.
Cytogenetic and Genome Research
|
January 9, 2013
Clinical impact of somatic mosaicism in cases with small supernumerary marker chromosomes
T Liehr, E Klein, K Mrasek, et al.
Molecular Human Reproduction
|
October 5, 2007
Breakpoint characterization: a new approach for segregation analysis of paracentric inversion in human sperm
S Bhatt, K Moradkhani, K Mrasek, et al.
American Journal of Medical Genetics. Part A
|
September 4, 2010
Characterization of a complex cryptic mosaicism for an sSMC derived from the X chromosome present in a boy with congenital malformations
M Santos, K Mrasek, I Madrigal, et al.
Cytogenetic and Genome Research
|
September 7, 2006
De novostructural chromosomal imbalances: molecular cytogenetic characterization of partial trisomies
A Dufke, S Singer, S Borell-Kost, et al.
Balkan Journal of Medical Genetics : BJMG
|
September 21, 2013
Evidence for correlation of fragile sites and chromosomal breakpoints in carriers of constitutional balanced chromosomal rearrangements
T Liehr, N Kosayakova, J Schröder, et al.
Cytogenetic and Genome Research
|
November 13, 2013
Inverted segment size and the presence of recombination hot spot clusters matter in sperm segregation analysis
S S Bhatt, M Manvelyan, K Moradkhani, et al.
International Journal of Molecular Medicine
|
January 22, 2008
Parental-origin-determination fluorescence in situ hybridization distinguishes homologous human chromosomes on a single-cell level
A Weise, M Gross, K Mrasek, et al.
Page
of 4
Search research articles
Search
Showing results (11-20 of 31) with videos related to
Sort By:
Page
of 4
Cytogenetic and Genome Research
|
March 9, 2004
Multitude multicolor chromosome banding (mMCB) - a comprehensive one-step multicolor FISH banding method
A Weise, A Heller, H Starke, et al.
Cytogenetic and Genome Research
|
November 20, 2002
Multicolor chromosome banding (MCB) with YAC/BAC-based probes and region-specific microdissection DNA libraries
T Liehr, A Weise, A Heller, et al.
Cytogenetic and Genome Research
|
September 7, 2006
Supernumerary marker chromosome 5 diagnosed by M-FISH in a child with congenital heart defect and unusual face
C Sarri, Y Gyftodimou, M Grigoriadou, et al.
Cytogenetic and Genome Research
|
January 9, 2013
Clinical impact of somatic mosaicism in cases with small supernumerary marker chromosomes
T Liehr, E Klein, K Mrasek, et al.
Molecular Human Reproduction
|
October 5, 2007
Breakpoint characterization: a new approach for segregation analysis of paracentric inversion in human sperm
S Bhatt, K Moradkhani, K Mrasek, et al.
American Journal of Medical Genetics. Part A
|
September 4, 2010
Characterization of a complex cryptic mosaicism for an sSMC derived from the X chromosome present in a boy with congenital malformations
M Santos, K Mrasek, I Madrigal, et al.
Cytogenetic and Genome Research
|
September 7, 2006
De novostructural chromosomal imbalances: molecular cytogenetic characterization of partial trisomies
A Dufke, S Singer, S Borell-Kost, et al.
Balkan Journal of Medical Genetics : BJMG
|
September 21, 2013
Evidence for correlation of fragile sites and chromosomal breakpoints in carriers of constitutional balanced chromosomal rearrangements
T Liehr, N Kosayakova, J Schröder, et al.
Cytogenetic and Genome Research
|
November 13, 2013
Inverted segment size and the presence of recombination hot spot clusters matter in sperm segregation analysis
S S Bhatt, M Manvelyan, K Moradkhani, et al.
International Journal of Molecular Medicine
|
January 22, 2008
Parental-origin-determination fluorescence in situ hybridization distinguishes homologous human chromosomes on a single-cell level
A Weise, M Gross, K Mrasek, et al.
Page
of 4