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Brynn Levy

Showing results (51-60 of 122) with videos related to

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Dermatology (Basel, Switzerland)|February 8, 2012
Copy number variations on chromosome 4q26-27 are associated with Cantu syndromeMazen Kurban, Chong Ae Kim, Maija Kiuru, et al.
Journal of Assisted Reproduction and Genetics|June 1, 2013
Incidental identification of balanced translocation carrier patients through comprehensive chromosome screening of IVF-derived blastocystsNathan R Treff, Eric J Forman, Mandy G Katz-Jaffe, et al.
Prenatal Diagnosis|July 7, 2016
The 2015 Malcolm Ferguson-Smith Young Investigator AwardAlessandro Ghidini, Diana W Bianchi, Brynn Levy, et al.
Cancer Biology & Therapy|February 9, 2016
Genome-wide analysis of abdominal and pleural malignant mesothelioma with DNA arrays reveals both common and distinct regions of copy number alterationAlain C Borczuk, Jianming Pei, Robert N Taub, et al.
Prenatal Diagnosis|January 26, 2025
Advances in Prenatal Cell-Free DNA Screening for Dominant Monogenic Conditions: A Review of Current Progress and Future Directions in Clinical ImplementationJun Liao, Naixin Xu, Harry Gao, et al.
American Journal of Medical Genetics. Part A|July 12, 2011
The proximal chromosome 14q microdeletion syndrome: delineation of the phenotype using high resolution SNP oligonucleotide microarray analysis (SOMA) and review of the literatureEdina Torgyekes, Alan L Shanske, Kwame Anyane-Yeboa, et al.
Prenatal Diagnosis|June 29, 2018
The 2017 Malcolm Ferguson-Smith Young Investigator AwardDiana W Bianchi, Alessandro Ghidini, Brynn Levy, et al.
Prenatal Diagnosis|August 16, 2019
The 2018 Malcolm Ferguson-Smith Young Investigator AwardDiana W Bianchi, Alessandro Ghidini, Brynn Levy, et al.
Molecular Genetics and Metabolism|April 13, 2010
Uncovering microdeletions in patients with severe Glut-1 deficiency syndrome using SNP oligonucleotide microarray analysisBrynn Levy, Dong Wang, Paivi M Ullner, et al.
Prenatal Diagnosis|June 30, 2020
The 2019 Malcolm Ferguson-Smith Young Investigator AwardDiana W Bianchi, Jan Deprest, Brynn Levy, et al.
Pageof 13

Showing results (51-60 of 122) with videos related to

Sort By:
Pageof 13
Dermatology (Basel, Switzerland)|February 8, 2012
Copy number variations on chromosome 4q26-27 are associated with Cantu syndromeMazen Kurban, Chong Ae Kim, Maija Kiuru, et al.
Journal of Assisted Reproduction and Genetics|June 1, 2013
Incidental identification of balanced translocation carrier patients through comprehensive chromosome screening of IVF-derived blastocystsNathan R Treff, Eric J Forman, Mandy G Katz-Jaffe, et al.
Prenatal Diagnosis|July 7, 2016
The 2015 Malcolm Ferguson-Smith Young Investigator AwardAlessandro Ghidini, Diana W Bianchi, Brynn Levy, et al.
Cancer Biology & Therapy|February 9, 2016
Genome-wide analysis of abdominal and pleural malignant mesothelioma with DNA arrays reveals both common and distinct regions of copy number alterationAlain C Borczuk, Jianming Pei, Robert N Taub, et al.
Prenatal Diagnosis|January 26, 2025
Advances in Prenatal Cell-Free DNA Screening for Dominant Monogenic Conditions: A Review of Current Progress and Future Directions in Clinical ImplementationJun Liao, Naixin Xu, Harry Gao, et al.
American Journal of Medical Genetics. Part A|July 12, 2011
The proximal chromosome 14q microdeletion syndrome: delineation of the phenotype using high resolution SNP oligonucleotide microarray analysis (SOMA) and review of the literatureEdina Torgyekes, Alan L Shanske, Kwame Anyane-Yeboa, et al.
Prenatal Diagnosis|June 29, 2018
The 2017 Malcolm Ferguson-Smith Young Investigator AwardDiana W Bianchi, Alessandro Ghidini, Brynn Levy, et al.
Prenatal Diagnosis|August 16, 2019
The 2018 Malcolm Ferguson-Smith Young Investigator AwardDiana W Bianchi, Alessandro Ghidini, Brynn Levy, et al.
Molecular Genetics and Metabolism|April 13, 2010
Uncovering microdeletions in patients with severe Glut-1 deficiency syndrome using SNP oligonucleotide microarray analysisBrynn Levy, Dong Wang, Paivi M Ullner, et al.
Prenatal Diagnosis|June 30, 2020
The 2019 Malcolm Ferguson-Smith Young Investigator AwardDiana W Bianchi, Jan Deprest, Brynn Levy, et al.
Pageof 13