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Blake C Ballif

Showing results (11-20 of 83) with videos related to

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Human Genetics|October 2, 2021
Identification of a novel missense mutation in the fibroblast growth factor 5 gene associated with longhair in the Maine Coon CatGriffin D Shaffer, Blake C Ballif, Kathryn Meurs, et al.
Journal of Veterinary Diagnostic Investigation : Official Publication of the American Association of Veterinary Laboratory Diagnosticians, Inc|January 22, 2019
Canine factor VII deficiency: lessons learned in applying methods-based laboratory proficiency testingChristina J Ramirez, Melissa Krug, Adam Zahand, et al.
Molecular Cytogenetics|July 1, 2010
Comparative analysis of copy number detection by whole-genome BAC and oligonucleotide array CGHNicholas J Neill, Beth S Torchia, Bassem A Bejjani, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|October 3, 2007
The identification of microdeletion syndromes and other chromosome abnormalities: cytogenetic methods of the past, new technologies for the futureLisa G Shaffer, Bassem A Bejjani, Beth Torchia, et al.
Expert Opinion on Medical Diagnostics|March 15, 2013
In the middle of it all: a centered approach to chromosome analysisLisa G Shaffer, Blake C Ballif, Aaron Theisen, et al.
Methods in Molecular Medicine|October 31, 2006
Comparative genomic hybridization by microarray for the detection of cytogenetic imbalanceMalgorzata Jarmuz, Blake C Ballif, Catherine D Kashork, et al.
Human Genetics|July 19, 2006
Identification of sequence motifs at the breakpoint junctions in three t(1;9)(p36.3;q34) and delineation of mechanisms involved in generating balanced translocationsMarzena Gajecka, Adam Pavlicek, Caron D Glotzbach, et al.
Prenatal Diagnosis|July 23, 2008
Comparison of microarray-based detection rates for cytogenetic abnormalities in prenatal and neonatal specimensLisa G Shaffer, Justine Coppinger, Sarah Alliman, et al.
The Journal of Pediatrics|July 25, 2006
Targeted genomic microarray analysis for identification of chromosome abnormalities in 1500 consecutive clinical casesLisa G Shaffer, Catherine D Kashork, Reza Saleki, et al.
Prenatal Diagnosis|February 24, 2006
Detecting sex chromosome anomalies and common triploidies in products of conception by array-based comparative genomic hybridizationBlake C Ballif, Catherine D Kashork, Reza Saleki, et al.
Pageof 9

Showing results (11-20 of 83) with videos related to

Sort By:
Pageof 9
Human Genetics|October 2, 2021
Identification of a novel missense mutation in the fibroblast growth factor 5 gene associated with longhair in the Maine Coon CatGriffin D Shaffer, Blake C Ballif, Kathryn Meurs, et al.
Journal of Veterinary Diagnostic Investigation : Official Publication of the American Association of Veterinary Laboratory Diagnosticians, Inc|January 22, 2019
Canine factor VII deficiency: lessons learned in applying methods-based laboratory proficiency testingChristina J Ramirez, Melissa Krug, Adam Zahand, et al.
Molecular Cytogenetics|July 1, 2010
Comparative analysis of copy number detection by whole-genome BAC and oligonucleotide array CGHNicholas J Neill, Beth S Torchia, Bassem A Bejjani, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|October 3, 2007
The identification of microdeletion syndromes and other chromosome abnormalities: cytogenetic methods of the past, new technologies for the futureLisa G Shaffer, Bassem A Bejjani, Beth Torchia, et al.
Expert Opinion on Medical Diagnostics|March 15, 2013
In the middle of it all: a centered approach to chromosome analysisLisa G Shaffer, Blake C Ballif, Aaron Theisen, et al.
Methods in Molecular Medicine|October 31, 2006
Comparative genomic hybridization by microarray for the detection of cytogenetic imbalanceMalgorzata Jarmuz, Blake C Ballif, Catherine D Kashork, et al.
Human Genetics|July 19, 2006
Identification of sequence motifs at the breakpoint junctions in three t(1;9)(p36.3;q34) and delineation of mechanisms involved in generating balanced translocationsMarzena Gajecka, Adam Pavlicek, Caron D Glotzbach, et al.
Prenatal Diagnosis|July 23, 2008
Comparison of microarray-based detection rates for cytogenetic abnormalities in prenatal and neonatal specimensLisa G Shaffer, Justine Coppinger, Sarah Alliman, et al.
The Journal of Pediatrics|July 25, 2006
Targeted genomic microarray analysis for identification of chromosome abnormalities in 1500 consecutive clinical casesLisa G Shaffer, Catherine D Kashork, Reza Saleki, et al.
Prenatal Diagnosis|February 24, 2006
Detecting sex chromosome anomalies and common triploidies in products of conception by array-based comparative genomic hybridizationBlake C Ballif, Catherine D Kashork, Reza Saleki, et al.
Pageof 9