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Daynna J Wolff

Showing results (1-10 of 57) with videos related to

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Cancer Genetics and Cytogenetics|June 15, 2006
Pediatric T-cell acute lymphoblastic leukemia with aberrations of both MLL lociDenise I Quigley, Daynna J Wolff
Methods in Molecular Biology (Clifton, N.J.)|January 17, 2019
Whole-Genome Single Nucleotide Polymorphism Microarray for Copy Number and Loss of Heterozygosity Analysis in TumorsRoss Rowsey, Iya Znoyko, Daynna J Wolff
Journal of the Association of Genetic Technologists|July 17, 2007
The Prothrombin 20209C>T Sequence Variant: To Test or Not to TestDenise I Quigley, Jessica K Booker, Daynna J Wolff
Archives of Pathology & Laboratory Medicine|July 8, 2011
Mitochondrial disorders of DNA polymerase γ dysfunction: from anatomic to molecular pathology diagnosisLinsheng Zhang, Sherine S L Chan, Daynna J Wolff
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 13, 2002
Pilot assessment of the subtelomeric regions of children with autism: detection of a 2q deletionDaynna J Wolff, Kimberly Clifton, Cynthia Karr, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 19, 2010
Laboratory guideline for Turner syndromeDaynna J Wolff, Daniel L Van Dyke, Cynthia M Powell, et al.
Expert Review of Molecular Diagnostics|December 26, 2006
HER2 testing: a review of detection methodologies and their clinical performanceJennifer Laudadio, Denise I Quigley, Raymond Tubbs, et al.
Archives of Pathology & Laboratory Medicine|January 3, 2012
Validation of fluorescence in situ hybridization using an analyte-specific reagent for detection of abnormalities involving the mixed lineage leukemia geneDebra F Saxe, Diane L Persons, Daynna J Wolff, et al.
Journal of the Association of Genetic Technologists|November 28, 2012
Cytogenetics caseload survey summary 2012Denise I Quigley, Joyce A Foster, Stephanie N Carter, et al.
The Journal of Molecular Diagnostics : JMD|January 27, 2006
Detection of an apparent homozygous 3120G>A cystic fibrosis mutation on a routine carrier screenDenise LaMarche Heaney, Patrick Flume, Lauren Hamilton, et al.
Pageof 6

Showing results (1-10 of 57) with videos related to

Sort By:
Pageof 6
Cancer Genetics and Cytogenetics|June 15, 2006
Pediatric T-cell acute lymphoblastic leukemia with aberrations of both MLL lociDenise I Quigley, Daynna J Wolff
Methods in Molecular Biology (Clifton, N.J.)|January 17, 2019
Whole-Genome Single Nucleotide Polymorphism Microarray for Copy Number and Loss of Heterozygosity Analysis in TumorsRoss Rowsey, Iya Znoyko, Daynna J Wolff
Journal of the Association of Genetic Technologists|July 17, 2007
The Prothrombin 20209C>T Sequence Variant: To Test or Not to TestDenise I Quigley, Jessica K Booker, Daynna J Wolff
Archives of Pathology & Laboratory Medicine|July 8, 2011
Mitochondrial disorders of DNA polymerase γ dysfunction: from anatomic to molecular pathology diagnosisLinsheng Zhang, Sherine S L Chan, Daynna J Wolff
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 13, 2002
Pilot assessment of the subtelomeric regions of children with autism: detection of a 2q deletionDaynna J Wolff, Kimberly Clifton, Cynthia Karr, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 19, 2010
Laboratory guideline for Turner syndromeDaynna J Wolff, Daniel L Van Dyke, Cynthia M Powell, et al.
Expert Review of Molecular Diagnostics|December 26, 2006
HER2 testing: a review of detection methodologies and their clinical performanceJennifer Laudadio, Denise I Quigley, Raymond Tubbs, et al.
Archives of Pathology & Laboratory Medicine|January 3, 2012
Validation of fluorescence in situ hybridization using an analyte-specific reagent for detection of abnormalities involving the mixed lineage leukemia geneDebra F Saxe, Diane L Persons, Daynna J Wolff, et al.
Journal of the Association of Genetic Technologists|November 28, 2012
Cytogenetics caseload survey summary 2012Denise I Quigley, Joyce A Foster, Stephanie N Carter, et al.
The Journal of Molecular Diagnostics : JMD|January 27, 2006
Detection of an apparent homozygous 3120G>A cystic fibrosis mutation on a routine carrier screenDenise LaMarche Heaney, Patrick Flume, Lauren Hamilton, et al.
Pageof 6