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Elizabeth C Chao

Showing results (1-10 of 36) with videos related to

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Nucleic Acids Research|February 9, 2006
Molecular models for the tissue specificity of DNA mismatch repair-deficient carcinogenesisElizabeth C Chao, Steven M Lipkin
Familial Cancer|February 26, 2015
The importance of proper bioinformatics analysis and clinical interpretation of tumor genomic profiling: a case study of undifferentiated sarcoma and a constitutional pathogenic BRCA2 mutation and an MLH1 variant of uncertain significanceElizabeth Varga, Elizabeth C Chao, Nicholas D Yeager
Human Genetics|April 24, 2010
Update on molecular diagnosis of hereditary hemorrhagic telangiectasiaJennifer Richards-Yutz, Kathleen Grant, Elizabeth C Chao, et al.
Cancer Genetics|October 19, 2016
Breast cancer risk is similar for CHEK2 founder and non-founder mutation carriersTracey P Leedom, Holly LaDuca, Rachel McFarland, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 12, 2013
Patient decisions for disclosure of secondary findings among the first 200 individuals undergoing clinical diagnostic exome sequencingLayla Shahmirzadi, Elizabeth C Chao, Erika Palmaer, et al.
Gynecologic Oncology|January 28, 2015
Hereditary predisposition to ovarian cancer, looking beyond BRCA1/BRCA2Lindsey E Minion, Jill S Dolinsky, Dana M Chase, et al.
American Journal of Medical Genetics. Part A|April 8, 2015
ELP2 is a novel gene implicated in neurodevelopmental disabilitiesJulie S Cohen, Siddharth Srivastava, Kelly D Farwell, et al.
Gynecologic Oncology|January 8, 2019
Women with breast and uterine cancer are more likely to harbor germline mutations than women with breast or uterine cancer alone: A case for expanded gene testingKelly Fulk, Michael R Milam, Shuwei Li, et al.
JIMD Reports|March 26, 2014
Diagnostic Exome Sequencing and Tailored Bioinformatics of the Parents of a Deceased Child with Cobalamin Deficiency Suggests Digenic Inheritance of the MTR and LMBRD1 GenesKelly D Farwell Gonzalez, Xiang Li, Hsiao-Mei Lu, et al.
Plos One|February 3, 2017
Exome sequencing covers >98% of mutations identified on targeted next generation sequencing panelsHolly LaDuca, Kelly D Farwell, Huy Vuong, et al.
Pageof 4

Showing results (1-10 of 36) with videos related to

Sort By:
Pageof 4
Nucleic Acids Research|February 9, 2006
Molecular models for the tissue specificity of DNA mismatch repair-deficient carcinogenesisElizabeth C Chao, Steven M Lipkin
Familial Cancer|February 26, 2015
The importance of proper bioinformatics analysis and clinical interpretation of tumor genomic profiling: a case study of undifferentiated sarcoma and a constitutional pathogenic BRCA2 mutation and an MLH1 variant of uncertain significanceElizabeth Varga, Elizabeth C Chao, Nicholas D Yeager
Human Genetics|April 24, 2010
Update on molecular diagnosis of hereditary hemorrhagic telangiectasiaJennifer Richards-Yutz, Kathleen Grant, Elizabeth C Chao, et al.
Cancer Genetics|October 19, 2016
Breast cancer risk is similar for CHEK2 founder and non-founder mutation carriersTracey P Leedom, Holly LaDuca, Rachel McFarland, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 12, 2013
Patient decisions for disclosure of secondary findings among the first 200 individuals undergoing clinical diagnostic exome sequencingLayla Shahmirzadi, Elizabeth C Chao, Erika Palmaer, et al.
Gynecologic Oncology|January 28, 2015
Hereditary predisposition to ovarian cancer, looking beyond BRCA1/BRCA2Lindsey E Minion, Jill S Dolinsky, Dana M Chase, et al.
American Journal of Medical Genetics. Part A|April 8, 2015
ELP2 is a novel gene implicated in neurodevelopmental disabilitiesJulie S Cohen, Siddharth Srivastava, Kelly D Farwell, et al.
Gynecologic Oncology|January 8, 2019
Women with breast and uterine cancer are more likely to harbor germline mutations than women with breast or uterine cancer alone: A case for expanded gene testingKelly Fulk, Michael R Milam, Shuwei Li, et al.
JIMD Reports|March 26, 2014
Diagnostic Exome Sequencing and Tailored Bioinformatics of the Parents of a Deceased Child with Cobalamin Deficiency Suggests Digenic Inheritance of the MTR and LMBRD1 GenesKelly D Farwell Gonzalez, Xiang Li, Hsiao-Mei Lu, et al.
Plos One|February 3, 2017
Exome sequencing covers >98% of mutations identified on targeted next generation sequencing panelsHolly LaDuca, Kelly D Farwell, Huy Vuong, et al.
Pageof 4