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Tracy Brandt

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Molecular Genetics and Genomics : MGG|August 22, 2008
The Lawc protein is required for proper transcription by RNA polymerase II in DrosophilaTracy Brandt, Victor G Corces
Human Molecular Genetics|June 24, 2010
Large inverted repeats within Xp11.2 are present at the breakpoints of isodicentric X chromosomes in Turner syndromeStuart A Scott, Ninette Cohen, Tracy Brandt, et al.
European Journal of Medical Genetics|September 24, 2013
46,XY disorder of sex development and developmental delay associated with a novel 9q33.3 microdeletion encompassing NR5A1Tracy Brandt, Leah Blanchard, Khyati Desai, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 20, 2010
Detection of low-level mosaicism and placental mosaicism by oligonucleotide array comparative genomic hybridizationStuart A Scott, Ninette Cohen, Tracy Brandt, et al.
American Journal of Human Genetics|October 7, 2025
A scalable approach for genomic-first rare disorder detection in a healthcare-based populationRebecca I Torene, Karyn Meltz Murphy, Tracy Brandt, et al.
Clinical Genetics|November 14, 2019
Sorting nexin 27 (SNX27) variants associated with seizures, developmental delay, behavioral disturbance, and subcortical brain abnormalitiesDaniel J Parente, Stephanie M Morris, Robert C McKinstry, et al.
American Journal of Medical Genetics. Part A|April 11, 2012
Complex autism spectrum disorder in a patient with a 17q12 microduplicationTracy Brandt, Khyati Desai, David Grodberg, et al.
BMC Medical Genomics|April 25, 2014
Analytical validation of whole exome and whole genome sequencing for clinical applicationsMichael D Linderman, Tracy Brandt, Lisa Edelmann, et al.
Epilepsia|April 15, 2018
Diagnostic outcomes for genetic testing of 70 genes in 8565 patients with epilepsy and neurodevelopmental disordersAmanda S Lindy, Mary Beth Stosser, Elizabeth Butler, et al.
Molecular Autism|August 4, 2010
A large-scale survey of the novel 15q24 microdeletion syndrome in autism spectrum disorders identifies an atypical deletion that narrows the critical regionL Alison McInnes, Alisa Nakamine, Marion Pilorge, et al.
Pageof 2

Showing results (1-10 of 20) with videos related to

Sort By:
Pageof 2
Molecular Genetics and Genomics : MGG|August 22, 2008
The Lawc protein is required for proper transcription by RNA polymerase II in DrosophilaTracy Brandt, Victor G Corces
Human Molecular Genetics|June 24, 2010
Large inverted repeats within Xp11.2 are present at the breakpoints of isodicentric X chromosomes in Turner syndromeStuart A Scott, Ninette Cohen, Tracy Brandt, et al.
European Journal of Medical Genetics|September 24, 2013
46,XY disorder of sex development and developmental delay associated with a novel 9q33.3 microdeletion encompassing NR5A1Tracy Brandt, Leah Blanchard, Khyati Desai, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 20, 2010
Detection of low-level mosaicism and placental mosaicism by oligonucleotide array comparative genomic hybridizationStuart A Scott, Ninette Cohen, Tracy Brandt, et al.
American Journal of Human Genetics|October 7, 2025
A scalable approach for genomic-first rare disorder detection in a healthcare-based populationRebecca I Torene, Karyn Meltz Murphy, Tracy Brandt, et al.
Clinical Genetics|November 14, 2019
Sorting nexin 27 (SNX27) variants associated with seizures, developmental delay, behavioral disturbance, and subcortical brain abnormalitiesDaniel J Parente, Stephanie M Morris, Robert C McKinstry, et al.
American Journal of Medical Genetics. Part A|April 11, 2012
Complex autism spectrum disorder in a patient with a 17q12 microduplicationTracy Brandt, Khyati Desai, David Grodberg, et al.
BMC Medical Genomics|April 25, 2014
Analytical validation of whole exome and whole genome sequencing for clinical applicationsMichael D Linderman, Tracy Brandt, Lisa Edelmann, et al.
Epilepsia|April 15, 2018
Diagnostic outcomes for genetic testing of 70 genes in 8565 patients with epilepsy and neurodevelopmental disordersAmanda S Lindy, Mary Beth Stosser, Elizabeth Butler, et al.
Molecular Autism|August 4, 2010
A large-scale survey of the novel 15q24 microdeletion syndrome in autism spectrum disorders identifies an atypical deletion that narrows the critical regionL Alison McInnes, Alisa Nakamine, Marion Pilorge, et al.
Pageof 2