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Blake C Ballif

Showing results (1-10 of 83) with videos related to

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Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|April 1, 2004
Monosomy 1p36 breakpoints indicate repetitive DNA sequence elements may be involved in generating and/or stabilizing some terminal deletionsBlake C Ballif, Marzena Gajecka, Lisa G Shaffer
Current Opinion in Genetics & Development|February 17, 2012
The use of new technologies in the detection of balanced translocations in hematologic disordersLisa G Shaffer, Roger A Schultz, Blake C Ballif
Methods in Molecular Biology (Clifton, N.J.)|March 11, 2010
The use of microarray technology for cytogeneticsBassem A Bejjani, Lisa G Shaffer, Blake C Ballif
Methods in Molecular Biology (Clifton, N.J.)|February 16, 2013
The use of cytogenetic microarrays in myelodysplastic syndrome characterizationLisa G Shaffer, Blake C Ballif, Roger A Schultz
Human Genetics|October 28, 2003
Translocation breakpoint mapping and sequence analysis in three monosomy 1p36 subjects with der(1)t(1;1)(p36;q44) suggest mechanisms for telomere capture in stabilizing de novo terminal rearrangementsBlake C Ballif, Keiko Wakui, Marzena Gajecka, et al.
Expert Review of Molecular Diagnostics|June 7, 2005
Array-based comparative genomic hybridization in clinical diagnosisBassem A Bejjani, Aaron P Theisen, Blake C Ballif, et al.
Human Genetics|July 21, 2021
Identification of aneuploidy in dogs screened by a SNP microarrayLisa G Shaffer, Bradley Hopp, Marek Switonski, et al.
European Journal of Human Genetics : EJHG|August 31, 2006
Identification of cryptic imbalance in phenotypically normal and abnormal translocation carriersMarzena Gajecka, Caron D Glotzbach, Malgorzata Jarmuz, et al.
Human Genetics|April 15, 2019
Quality assurance checklist and additional considerations for canine clinical genetic testing laboratories: a follow-up to the published standards and guidelinesLisa G Shaffer, Anja Geretschlaeger, Christina J Ramirez, et al.
Human Molecular Genetics|August 14, 2003
Monosomy 1p36 breakpoint junctions suggest pre-meiotic breakage-fusion-bridge cycles are involved in generating terminal deletionsBlake C Ballif, Wei Yu, Chad A Shaw, et al.
Pageof 9

Showing results (1-10 of 83) with videos related to

Sort By:
Pageof 9
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|April 1, 2004
Monosomy 1p36 breakpoints indicate repetitive DNA sequence elements may be involved in generating and/or stabilizing some terminal deletionsBlake C Ballif, Marzena Gajecka, Lisa G Shaffer
Current Opinion in Genetics & Development|February 17, 2012
The use of new technologies in the detection of balanced translocations in hematologic disordersLisa G Shaffer, Roger A Schultz, Blake C Ballif
Methods in Molecular Biology (Clifton, N.J.)|March 11, 2010
The use of microarray technology for cytogeneticsBassem A Bejjani, Lisa G Shaffer, Blake C Ballif
Methods in Molecular Biology (Clifton, N.J.)|February 16, 2013
The use of cytogenetic microarrays in myelodysplastic syndrome characterizationLisa G Shaffer, Blake C Ballif, Roger A Schultz
Human Genetics|October 28, 2003
Translocation breakpoint mapping and sequence analysis in three monosomy 1p36 subjects with der(1)t(1;1)(p36;q44) suggest mechanisms for telomere capture in stabilizing de novo terminal rearrangementsBlake C Ballif, Keiko Wakui, Marzena Gajecka, et al.
Expert Review of Molecular Diagnostics|June 7, 2005
Array-based comparative genomic hybridization in clinical diagnosisBassem A Bejjani, Aaron P Theisen, Blake C Ballif, et al.
Human Genetics|July 21, 2021
Identification of aneuploidy in dogs screened by a SNP microarrayLisa G Shaffer, Bradley Hopp, Marek Switonski, et al.
European Journal of Human Genetics : EJHG|August 31, 2006
Identification of cryptic imbalance in phenotypically normal and abnormal translocation carriersMarzena Gajecka, Caron D Glotzbach, Malgorzata Jarmuz, et al.
Human Genetics|April 15, 2019
Quality assurance checklist and additional considerations for canine clinical genetic testing laboratories: a follow-up to the published standards and guidelinesLisa G Shaffer, Anja Geretschlaeger, Christina J Ramirez, et al.
Human Molecular Genetics|August 14, 2003
Monosomy 1p36 breakpoint junctions suggest pre-meiotic breakage-fusion-bridge cycles are involved in generating terminal deletionsBlake C Ballif, Wei Yu, Chad A Shaw, et al.
Pageof 9