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Blake C Ballif

Showing results (41-50 of 83) with videos related to

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American Journal of Human Genetics|April 11, 2003
Physical map of 1p36, placement of breakpoints in monosomy 1p36, and clinical characterization of the syndromeHeidi A Heilstedt, Blake C Ballif, Leslie A Howard, et al.
American Journal of Medical Genetics. Part A|April 9, 2009
aCGH detects partial tetrasomy of 12p in blood from Pallister-Killian syndrome cases without invasive skin biopsyAaron Theisen, Jill A Rosenfeld, Sandra A Farrell, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 7, 2012
Defining the impact of maternal cell contamination on the interpretation of prenatal microarray analysisAllen N Lamb, Jill A Rosenfeld, Justine Coppinger, et al.
Molecular Cytogenetics|February 5, 2011
Evaluation of chronic lymphocytic leukemia by BAC-based microarray analysisRoger A Schultz, Maria Delioukina, Karl Gaal, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 18, 2007
The discovery of microdeletion syndromes in the post-genomic era: review of the methodology and characterization of a new 1q41q42 microdeletion syndromeLisa G Shaffer, Aaron Theisen, Bassem A Bejjani, et al.
Cancer Genetics|December 28, 2011
Microarray-based comparative genomic hybridization of cancer targets reveals novel, recurrent genetic aberrations in the myelodysplastic syndromesKathryn A Kolquist, Roger A Schultz, Aubry Furrow, et al.
Molecular Cytogenetics|November 17, 2010
Assessing karyotype precision by microarray-based comparative genomic hybridization in the myelodysplastic/myeloproliferative syndromesMarilyn L Slovak, David D Smith, Victoria Bedell, et al.
Prenatal Diagnosis|August 1, 2012
Detection rates of clinically significant genomic alterations by microarray analysis for specific anomalies detected by ultrasoundLisa G Shaffer, Jill A Rosenfeld, Mindy P Dabell, et al.
Prenatal Diagnosis|August 7, 2012
Experience with microarray-based comparative genomic hybridization for prenatal diagnosis in over 5000 pregnanciesLisa G Shaffer, Mindy P Dabell, Allan J Fisher, et al.
American Journal of Medical Genetics. Part A|July 17, 2010
Refinement of causative genes in monosomy 1p36 through clinical and molecular cytogenetic characterization of small interstitial deletionsJill A Rosenfeld, John A Crolla, Susan Tomkins, et al.
Pageof 9

Showing results (41-50 of 83) with videos related to

Sort By:
Pageof 9
American Journal of Human Genetics|April 11, 2003
Physical map of 1p36, placement of breakpoints in monosomy 1p36, and clinical characterization of the syndromeHeidi A Heilstedt, Blake C Ballif, Leslie A Howard, et al.
American Journal of Medical Genetics. Part A|April 9, 2009
aCGH detects partial tetrasomy of 12p in blood from Pallister-Killian syndrome cases without invasive skin biopsyAaron Theisen, Jill A Rosenfeld, Sandra A Farrell, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 7, 2012
Defining the impact of maternal cell contamination on the interpretation of prenatal microarray analysisAllen N Lamb, Jill A Rosenfeld, Justine Coppinger, et al.
Molecular Cytogenetics|February 5, 2011
Evaluation of chronic lymphocytic leukemia by BAC-based microarray analysisRoger A Schultz, Maria Delioukina, Karl Gaal, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 18, 2007
The discovery of microdeletion syndromes in the post-genomic era: review of the methodology and characterization of a new 1q41q42 microdeletion syndromeLisa G Shaffer, Aaron Theisen, Bassem A Bejjani, et al.
Cancer Genetics|December 28, 2011
Microarray-based comparative genomic hybridization of cancer targets reveals novel, recurrent genetic aberrations in the myelodysplastic syndromesKathryn A Kolquist, Roger A Schultz, Aubry Furrow, et al.
Molecular Cytogenetics|November 17, 2010
Assessing karyotype precision by microarray-based comparative genomic hybridization in the myelodysplastic/myeloproliferative syndromesMarilyn L Slovak, David D Smith, Victoria Bedell, et al.
Prenatal Diagnosis|August 1, 2012
Detection rates of clinically significant genomic alterations by microarray analysis for specific anomalies detected by ultrasoundLisa G Shaffer, Jill A Rosenfeld, Mindy P Dabell, et al.
Prenatal Diagnosis|August 7, 2012
Experience with microarray-based comparative genomic hybridization for prenatal diagnosis in over 5000 pregnanciesLisa G Shaffer, Mindy P Dabell, Allan J Fisher, et al.
American Journal of Medical Genetics. Part A|July 17, 2010
Refinement of causative genes in monosomy 1p36 through clinical and molecular cytogenetic characterization of small interstitial deletionsJill A Rosenfeld, John A Crolla, Susan Tomkins, et al.
Pageof 9