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Peter R Papenhausen

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Experimental and Molecular Pathology|July 20, 2005
Oncogene amplification in transforming myelodysplasiaPeter R Papenhausen, Sharon Griffin, James Tepperberg
Cytogenetic and Genome Research|November 18, 2014
Four-copy number intervals in SNP microarray analysis: unique patterns and positionsPeter R Papenhausen, Carla A Kelly, Val Zvereff, et al.
Journal of Hematopathology|January 4, 2024
B-lymphoblastic leukemia/lymphoma with MYC and BCL2 gene rearrangements shows evidence for clonal evolution and mitotic recombinationSteven A Schichman, Andrea L Penton, Sai Nikhila Ghanta, et al.
Annals of Clinical and Laboratory Science|July 5, 2018
Discrepant Cytogenetic and Interphase Fluorescence In Situ Hybridization (I-FISH) Results from Bone Marrow Specimens of Patients with Hematologic NeoplasmsEduardo S Cantú, Henry Dong, David R Forsyth, et al.
Molecular Cytogenetics|July 21, 2021
Clinical significance and mechanisms associated with segmental UPDPeter R Papenhausen, Carla A Kelly, Samuel Harris, et al.
Prenatal Diagnosis|August 30, 2018
Monosomy X rescue explains discordant NIPT results and leads to uniparental isodisomyM Katharine Rudd, Justin B Schleede, Sabrina R Williams, et al.
Chromosoma|August 10, 2011
Formation of novel CENP-A domains on tandem repetitive DNA and across chromosome breakpoints on human chromosome 8q21 neocentromeresDan Hasson, Alicia Alonso, Fanny Cheung, et al.
Prenatal Diagnosis|April 1, 2024
Prenatal detection of mosaicism for a genome wide uniparental disomy cell line in a cohort of patients: Implications and outcomesMargriet Johansen, Gloria T Haskell, Alexandra Arreola, et al.
Molecular Genetics and Metabolism|June 27, 2013
Severe obesity and diabetes insipidus in a patient with PCSK1 deficiencyGraeme R Frank, Joyce Fox, Ninfa Candela, et al.
Orphanet Journal of Rare Diseases|February 14, 2007
Further phenotypic delineation of subtelomeric (terminal) 4q deletion with emphasis on intracranial and reproductive anatomyEric Scott Sills, M J Burns, Laurinda D Parker, et al.
Pageof 2

Showing results (1-10 of 17) with videos related to

Sort By:
Pageof 2
Experimental and Molecular Pathology|July 20, 2005
Oncogene amplification in transforming myelodysplasiaPeter R Papenhausen, Sharon Griffin, James Tepperberg
Cytogenetic and Genome Research|November 18, 2014
Four-copy number intervals in SNP microarray analysis: unique patterns and positionsPeter R Papenhausen, Carla A Kelly, Val Zvereff, et al.
Journal of Hematopathology|January 4, 2024
B-lymphoblastic leukemia/lymphoma with MYC and BCL2 gene rearrangements shows evidence for clonal evolution and mitotic recombinationSteven A Schichman, Andrea L Penton, Sai Nikhila Ghanta, et al.
Annals of Clinical and Laboratory Science|July 5, 2018
Discrepant Cytogenetic and Interphase Fluorescence In Situ Hybridization (I-FISH) Results from Bone Marrow Specimens of Patients with Hematologic NeoplasmsEduardo S Cantú, Henry Dong, David R Forsyth, et al.
Molecular Cytogenetics|July 21, 2021
Clinical significance and mechanisms associated with segmental UPDPeter R Papenhausen, Carla A Kelly, Samuel Harris, et al.
Prenatal Diagnosis|August 30, 2018
Monosomy X rescue explains discordant NIPT results and leads to uniparental isodisomyM Katharine Rudd, Justin B Schleede, Sabrina R Williams, et al.
Chromosoma|August 10, 2011
Formation of novel CENP-A domains on tandem repetitive DNA and across chromosome breakpoints on human chromosome 8q21 neocentromeresDan Hasson, Alicia Alonso, Fanny Cheung, et al.
Prenatal Diagnosis|April 1, 2024
Prenatal detection of mosaicism for a genome wide uniparental disomy cell line in a cohort of patients: Implications and outcomesMargriet Johansen, Gloria T Haskell, Alexandra Arreola, et al.
Molecular Genetics and Metabolism|June 27, 2013
Severe obesity and diabetes insipidus in a patient with PCSK1 deficiencyGraeme R Frank, Joyce Fox, Ninfa Candela, et al.
Orphanet Journal of Rare Diseases|February 14, 2007
Further phenotypic delineation of subtelomeric (terminal) 4q deletion with emphasis on intracranial and reproductive anatomyEric Scott Sills, M J Burns, Laurinda D Parker, et al.
Pageof 2