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Blake C Ballif

Showing results (31-40 of 83) with videos related to

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Plos Genetics|February 6, 2014
Large inverted duplications in the human genome form via a fold-back mechanismKaren E Hermetz, Scott Newman, Karen N Conneely, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 15, 2009
Impact of genotype-first diagnosis: the detection of microdeletion and microduplication syndromes with cancer predisposition by aCGHSara Anne Adams, Justine Coppinger, Sulagna C Saitta, et al.
American Journal of Medical Genetics. Part A|November 15, 2006
Detection of low-level mosaicism by array CGH in routine diagnostic specimensBlake C Ballif, Emily A Rorem, Kyle Sundin, et al.
Diagnostic Molecular Pathology : the American Journal of Surgical Pathology, Part B|February 2, 2013
Modified array-based comparative genomic hybridization detects cryptic and variant PML-RARA rearrangements in acute promyelocytic leukemia lacking classic translocationsAaron M Gruver, Heesun J Rogers, James R Cook, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 3, 2010
Copy number variations associated with autism spectrum disorders contribute to a spectrum of neurodevelopmental disordersJill A Rosenfeld, Blake C Ballif, Beth S Torchia, et al.
European Journal of Human Genetics : EJHG|February 10, 2012
Proximal microdeletions and microduplications of 1q21.1 contribute to variable abnormal phenotypesJill A Rosenfeld, Ryan N Traylor, G Bradley Schaefer, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 7, 2007
Development of a high-density pericentromeric region BAC clone set for the detection and characterization of small supernumerary marker chromosomes by array CGHBlake C Ballif, Sara A Hornor, Scott G Sulpizio, et al.
Prenatal Diagnosis|May 25, 2012
Referral patterns for microarray testing in prenatal diagnosisLisa G Shaffer, Mindy Preston Dabell, Jill A Rosenfeld, et al.
Genome Research|March 9, 2011
Recurrence, submicroscopic complexity, and potential clinical relevance of copy gains detected by array CGH that are shown to be unbalanced insertions by FISHNicholas J Neill, Blake C Ballif, Allen N Lamb, et al.
Prenatal Diagnosis|April 3, 2012
Referral patterns for microarray testing in prenatal diagnosisLisa G Shaffer, Mindy Preston Dabell, Jill A Rosenfeld, et al.
Pageof 9

Showing results (31-40 of 83) with videos related to

Sort By:
Pageof 9
Plos Genetics|February 6, 2014
Large inverted duplications in the human genome form via a fold-back mechanismKaren E Hermetz, Scott Newman, Karen N Conneely, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 15, 2009
Impact of genotype-first diagnosis: the detection of microdeletion and microduplication syndromes with cancer predisposition by aCGHSara Anne Adams, Justine Coppinger, Sulagna C Saitta, et al.
American Journal of Medical Genetics. Part A|November 15, 2006
Detection of low-level mosaicism by array CGH in routine diagnostic specimensBlake C Ballif, Emily A Rorem, Kyle Sundin, et al.
Diagnostic Molecular Pathology : the American Journal of Surgical Pathology, Part B|February 2, 2013
Modified array-based comparative genomic hybridization detects cryptic and variant PML-RARA rearrangements in acute promyelocytic leukemia lacking classic translocationsAaron M Gruver, Heesun J Rogers, James R Cook, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 3, 2010
Copy number variations associated with autism spectrum disorders contribute to a spectrum of neurodevelopmental disordersJill A Rosenfeld, Blake C Ballif, Beth S Torchia, et al.
European Journal of Human Genetics : EJHG|February 10, 2012
Proximal microdeletions and microduplications of 1q21.1 contribute to variable abnormal phenotypesJill A Rosenfeld, Ryan N Traylor, G Bradley Schaefer, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 7, 2007
Development of a high-density pericentromeric region BAC clone set for the detection and characterization of small supernumerary marker chromosomes by array CGHBlake C Ballif, Sara A Hornor, Scott G Sulpizio, et al.
Prenatal Diagnosis|May 25, 2012
Referral patterns for microarray testing in prenatal diagnosisLisa G Shaffer, Mindy Preston Dabell, Jill A Rosenfeld, et al.
Genome Research|March 9, 2011
Recurrence, submicroscopic complexity, and potential clinical relevance of copy gains detected by array CGH that are shown to be unbalanced insertions by FISHNicholas J Neill, Blake C Ballif, Allen N Lamb, et al.
Prenatal Diagnosis|April 3, 2012
Referral patterns for microarray testing in prenatal diagnosisLisa G Shaffer, Mindy Preston Dabell, Jill A Rosenfeld, et al.
Pageof 9