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Bradford C Powell

Showing results (1-10 of 45) with videos related to

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BMC Bioinformatics|January 21, 2006
Similarity-based gene detection: using COGs to find evolutionarily-conserved ORFsBradford C Powell, Clyde A Hutchison
JAMA|May 12, 2017
Finding the Rare Pathogenic Variants in a Human GenomeJames P Evans, Bradford C Powell, Jonathan S Berg
Journal of Bacteriology|June 22, 2005
Transcriptional analysis of the conserved ftsZ gene cluster in Mycoplasma genitalium and Mycoplasma pneumoniaeGwynedd A Benders, Bradford C Powell, Clyde A Hutchison
BMC Evolutionary Biology|February 18, 2006
Tracking the evolution of alternatively spliced exons within the Dscam familyMack E Crayton, Bradford C Powell, Todd J Vision, et al.
Journal of Pediatric Hematology/Oncology|August 10, 2020
Rosai-Dorfman Disease and Exocrine Pancreatic Insufficiency in a Patient With a Germline SLC29A3 MutationJulie Blatt, Preeti Parekh, Bradford C Powell, et al.
Annual Review of Genomics and Human Genetics|April 1, 2022
Establishing the Medical Actionability of Genomic VariantsKatrina A B Goddard, Kristy Lee, Adam H Buchanan, et al.
American Journal of Medical Genetics. Part A|September 5, 2024
WDR44 Loss-of-Function Promoter Deletion in a Male Newborn With a Ciliopathy PhenotypeTam P Sneddon, Kelly L Gilmore, Mai Xiong, et al.
Journal of Genetic Counseling|January 23, 2020
Referencing BRCA in hereditary cancer risk discussions: In search of an anchor in a sea of uncertaintyMargaret Waltz, Anya E R Prince, Julianne M O'Daniel, et al.
Genome Medicine|December 1, 2019
Comparative analysis of functional assay evidence use by ClinGen Variant Curation Expert PanelsDona M Kanavy, Shannon M McNulty, Meera K Jairath, et al.
Prenatal Diagnosis|July 15, 2021
Noninvasive prenatal exome sequencing diagnostic utility limited by sequencing depth and fetal fractionDayne L Filer, Piotr A Mieczkowski, Alicia Brandt, et al.
Pageof 5

Showing results (1-10 of 45) with videos related to

Sort By:
Pageof 5
BMC Bioinformatics|January 21, 2006
Similarity-based gene detection: using COGs to find evolutionarily-conserved ORFsBradford C Powell, Clyde A Hutchison
JAMA|May 12, 2017
Finding the Rare Pathogenic Variants in a Human GenomeJames P Evans, Bradford C Powell, Jonathan S Berg
Journal of Bacteriology|June 22, 2005
Transcriptional analysis of the conserved ftsZ gene cluster in Mycoplasma genitalium and Mycoplasma pneumoniaeGwynedd A Benders, Bradford C Powell, Clyde A Hutchison
BMC Evolutionary Biology|February 18, 2006
Tracking the evolution of alternatively spliced exons within the Dscam familyMack E Crayton, Bradford C Powell, Todd J Vision, et al.
Journal of Pediatric Hematology/Oncology|August 10, 2020
Rosai-Dorfman Disease and Exocrine Pancreatic Insufficiency in a Patient With a Germline SLC29A3 MutationJulie Blatt, Preeti Parekh, Bradford C Powell, et al.
Annual Review of Genomics and Human Genetics|April 1, 2022
Establishing the Medical Actionability of Genomic VariantsKatrina A B Goddard, Kristy Lee, Adam H Buchanan, et al.
American Journal of Medical Genetics. Part A|September 5, 2024
WDR44 Loss-of-Function Promoter Deletion in a Male Newborn With a Ciliopathy PhenotypeTam P Sneddon, Kelly L Gilmore, Mai Xiong, et al.
Journal of Genetic Counseling|January 23, 2020
Referencing BRCA in hereditary cancer risk discussions: In search of an anchor in a sea of uncertaintyMargaret Waltz, Anya E R Prince, Julianne M O'Daniel, et al.
Genome Medicine|December 1, 2019
Comparative analysis of functional assay evidence use by ClinGen Variant Curation Expert PanelsDona M Kanavy, Shannon M McNulty, Meera K Jairath, et al.
Prenatal Diagnosis|July 15, 2021
Noninvasive prenatal exome sequencing diagnostic utility limited by sequencing depth and fetal fractionDayne L Filer, Piotr A Mieczkowski, Alicia Brandt, et al.
Pageof 5