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Odelia Nahum

Showing results (1-10 of 13) with videos related to

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Methods in Molecular Biology (Clifton, N.J.)|December 4, 2018
DNA Extraction from Various Types of Prenatal SpecimensOdelia Nahum, Amanda Thomas, Brynn Levy
Methods in Molecular Biology (Clifton, N.J.)|December 4, 2018
Prenatal Diagnosis Using Chromosomal SNP MicroarraysMythily Ganapathi, Odelia Nahum, Brynn Levy
Methods in Molecular Biology (Clifton, N.J.)|December 4, 2018
Assessment of Maternal Cell Contamination in Prenatal Samples by Quantitative Fluorescent PCR (QF-PCR)Christie M Buchovecky, Odelia Nahum, Brynn Levy
Archives of Pathology & Laboratory Medicine|April 1, 2014
Genomic alterations in pulmonary adenocarcinoma in situ in an adolescent patientMarcela Salomao, Brynn Levy, Odelia Nahum, 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.
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.
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.
Oncotarget|May 21, 2016
Genetic landscape of T- and NK-cell post-transplant lymphoproliferative disordersElizabeth Margolskee, Vaidehi Jobanputra, Preti Jain, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 2, 2012
Tetrasomy 15q26: a distinct syndrome or Shprintzen-Goldberg syndrome phenocopy?Brynn Levy, David Tegay, Peter Papenhausen, et al.
Cancer Research|November 17, 2007
Deregulated overexpression of hCdt1 and hCdc6 promotes malignant behaviorMichalis Liontos, Marilena Koutsami, Maria Sideridou, et al.
Pageof 2

Showing results (1-10 of 13) with videos related to

Sort By:
Pageof 2
Methods in Molecular Biology (Clifton, N.J.)|December 4, 2018
DNA Extraction from Various Types of Prenatal SpecimensOdelia Nahum, Amanda Thomas, Brynn Levy
Methods in Molecular Biology (Clifton, N.J.)|December 4, 2018
Prenatal Diagnosis Using Chromosomal SNP MicroarraysMythily Ganapathi, Odelia Nahum, Brynn Levy
Methods in Molecular Biology (Clifton, N.J.)|December 4, 2018
Assessment of Maternal Cell Contamination in Prenatal Samples by Quantitative Fluorescent PCR (QF-PCR)Christie M Buchovecky, Odelia Nahum, Brynn Levy
Archives of Pathology & Laboratory Medicine|April 1, 2014
Genomic alterations in pulmonary adenocarcinoma in situ in an adolescent patientMarcela Salomao, Brynn Levy, Odelia Nahum, 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.
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.
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.
Oncotarget|May 21, 2016
Genetic landscape of T- and NK-cell post-transplant lymphoproliferative disordersElizabeth Margolskee, Vaidehi Jobanputra, Preti Jain, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 2, 2012
Tetrasomy 15q26: a distinct syndrome or Shprintzen-Goldberg syndrome phenocopy?Brynn Levy, David Tegay, Peter Papenhausen, et al.
Cancer Research|November 17, 2007
Deregulated overexpression of hCdt1 and hCdc6 promotes malignant behaviorMichalis Liontos, Marilena Koutsami, Maria Sideridou, et al.
Pageof 2