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J Ferber

Showing results (51-60 of 74) with videos related to

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Cancer Genetics and Cytogenetics|September 24, 2004
Positioning of cervical carcinoma and Burkitt lymphoma translocation breakpoints with respect to the human papillomavirus integration cluster in FRA8C at 8q24.13Matthew J Ferber, Paul Eilers, Ed Schuuring, et al.
Cold Spring Harbor Molecular Case Studies|May 11, 2017
Novel de novo variant in <i>EBF3</i> is likely to impact DNA binding in a patient with a neurodevelopmental disorder and expanded phenotypes: patient report, in silico functional assessment, and review of published casesPatrick R Blackburn, Sarah S Barnett, Michael T Zimmermann, et al.
Oncogene|October 17, 2003
Preferential integration of human papillomavirus type 18 near the c-myc locus in cervical carcinomaMatthew J Ferber, Erik C Thorland, Antoinette A T P Brink, et al.
Hereditary Cancer in Clinical Practice|February 5, 2015
High-grade endometrial stromal sarcoma as the initial presentation of an adult patient with Peutz-Jeghers Syndrome: a case reportMaria Fernanda Noriega-Iriondo, Gerardo Colon-Otero, Benjamin R Kipp, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 8, 2018
Determining the clinical validity of hereditary colorectal cancer and polyposis susceptibility genes using the Clinical Genome Resource Clinical Validity FrameworkBryce A Seifert, Jennifer L McGlaughon, Sarah A Jackson, et al.
Genetics in Medicine Open|December 13, 2024
Combining rare and common genetic variants improves population risk stratification for breast cancerAlexandre Bolze, Daniel Kiser, Kelly M Schiabor Barrett, et al.
Mayo Clinic Proceedings|June 20, 2014
Genomic medicine and incidental findings: balancing actionability and patient autonomyJennifer B McCormick, Richard R Sharp, Gianrico Farrugia, et al.
Oncogene|June 13, 2003
Integrations of the hepatitis B virus (HBV) and human papillomavirus (HPV) into the human telomerase reverse transcriptase (hTERT) gene in liver and cervical cancersM J Ferber, D P Montoya, C Yu, et al.
The Journal of Molecular Diagnostics : JMD|March 8, 2016
Preemptive Pharmacogenomic Testing for Precision Medicine: A Comprehensive Analysis of Five Actionable Pharmacogenomic Genes Using Next-Generation DNA Sequencing and a Customized CYP2D6 Genotyping CascadeYuan Ji, Jennifer M Skierka, Joseph H Blommel, et al.
Mayo Clinic Proceedings|October 6, 2015
Whole-Exome Sequencing of 10 Scientists: Evaluation of the Process and OutcomesNoralane M Lindor, Kimberly A Schahl, Kiley J Johnson, et al.
Pageof 8

Showing results (51-60 of 74) with videos related to

Sort By:
Pageof 8
Cancer Genetics and Cytogenetics|September 24, 2004
Positioning of cervical carcinoma and Burkitt lymphoma translocation breakpoints with respect to the human papillomavirus integration cluster in FRA8C at 8q24.13Matthew J Ferber, Paul Eilers, Ed Schuuring, et al.
Cold Spring Harbor Molecular Case Studies|May 11, 2017
Novel de novo variant in <i>EBF3</i> is likely to impact DNA binding in a patient with a neurodevelopmental disorder and expanded phenotypes: patient report, in silico functional assessment, and review of published casesPatrick R Blackburn, Sarah S Barnett, Michael T Zimmermann, et al.
Oncogene|October 17, 2003
Preferential integration of human papillomavirus type 18 near the c-myc locus in cervical carcinomaMatthew J Ferber, Erik C Thorland, Antoinette A T P Brink, et al.
Hereditary Cancer in Clinical Practice|February 5, 2015
High-grade endometrial stromal sarcoma as the initial presentation of an adult patient with Peutz-Jeghers Syndrome: a case reportMaria Fernanda Noriega-Iriondo, Gerardo Colon-Otero, Benjamin R Kipp, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 8, 2018
Determining the clinical validity of hereditary colorectal cancer and polyposis susceptibility genes using the Clinical Genome Resource Clinical Validity FrameworkBryce A Seifert, Jennifer L McGlaughon, Sarah A Jackson, et al.
Genetics in Medicine Open|December 13, 2024
Combining rare and common genetic variants improves population risk stratification for breast cancerAlexandre Bolze, Daniel Kiser, Kelly M Schiabor Barrett, et al.
Mayo Clinic Proceedings|June 20, 2014
Genomic medicine and incidental findings: balancing actionability and patient autonomyJennifer B McCormick, Richard R Sharp, Gianrico Farrugia, et al.
Oncogene|June 13, 2003
Integrations of the hepatitis B virus (HBV) and human papillomavirus (HPV) into the human telomerase reverse transcriptase (hTERT) gene in liver and cervical cancersM J Ferber, D P Montoya, C Yu, et al.
The Journal of Molecular Diagnostics : JMD|March 8, 2016
Preemptive Pharmacogenomic Testing for Precision Medicine: A Comprehensive Analysis of Five Actionable Pharmacogenomic Genes Using Next-Generation DNA Sequencing and a Customized CYP2D6 Genotyping CascadeYuan Ji, Jennifer M Skierka, Joseph H Blommel, et al.
Mayo Clinic Proceedings|October 6, 2015
Whole-Exome Sequencing of 10 Scientists: Evaluation of the Process and OutcomesNoralane M Lindor, Kimberly A Schahl, Kiley J Johnson, et al.
Pageof 8