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Wendy McKinnon

Showing results (1-10 of 26) with videos related to

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The Breast Journal|August 3, 2020
Risk for breast cancer and management of unaffected individuals with non-BRCA hereditary breast cancerMarie E Wood, Wendy McKinnon, Judy Garber
Journal of Genetic Counseling|June 28, 2007
Results of an intervention for individuals and families with BRCA mutations: a model for providing medical updates and psychosocial support following genetic testingWendy McKinnon, Shelly Naud, Taka Ashikaga, et al.
International Journal of Gynecological Pathology : Official Journal of the International Society of Gynecological Pathologists|April 25, 2024
Endometrial Cancer in a Family With RAD51D Gene MutationBrittany Gilmore, Linda Logan, Wendy McKinnon, et al.
Journal of the Association of Genetic Technologists|September 5, 2020
Acute Myeloid Leukemia with t(8;16)(p11.2;p13.3)/ KAT6A-CREBBP in a Patient with an NF1 Germline Mutation and Clinical Presentation Mimicking Acute Promyelocytic LeukemiaLiam Donnelly, Casey Rankins, Ximena Jordan Bruno, et al.
Human Pathology|October 25, 2011
Colonic ganglioneuromatous polyposis and metastatic adenocarcinoma in the setting of Cowden syndrome: a case report and literature reviewJoshua W Trufant, Laura Greene, Deborah L Cook, et al.
International Journal of Gynecological Pathology : Official Journal of the International Society of Gynecological Pathologists|February 12, 2022
Serous Tubal Intraepithelial Carcinoma in a Risk-reducing Salpingo-oophorectomy Specimen From a RAD51D Mutation Carrier: A Case ReportKalin J Gregory-Davis, Allison Walker, Laura S Colello, et al.
Journal of Cutaneous Pathology|December 14, 2011
Familial multiple pilomatrixomas as a presentation of attenuated adenomatosis polyposis coliJoshua Trufant, Wayne Kurz, Amylynne Frankel, et al.
Familial Cancer|May 26, 2009
Survey of unaffected BRCA and mismatch repair (MMR) mutation positive individualsWendy McKinnon, Kimberly C Banks, Joan Skelly, et al.
Human Mutation|April 23, 2002
A HOXA13 allele with a missense mutation in the homeobox and a dinucleotide deletion in the promoter underlies Guttmacher syndromeJeffrey W Innis, Frances R Goodman, Chiara Bacchelli, et al.
Psycho-Oncology|May 20, 2014
Intentions for risk-reducing surgery among high-risk women referred for BRCA1/BRCA2 genetic counselingAngie Tong, Scott Kelly, Rachel Nusbaum, et al.
Pageof 3

Showing results (1-10 of 26) with videos related to

Sort By:
Pageof 3
The Breast Journal|August 3, 2020
Risk for breast cancer and management of unaffected individuals with non-BRCA hereditary breast cancerMarie E Wood, Wendy McKinnon, Judy Garber
Journal of Genetic Counseling|June 28, 2007
Results of an intervention for individuals and families with BRCA mutations: a model for providing medical updates and psychosocial support following genetic testingWendy McKinnon, Shelly Naud, Taka Ashikaga, et al.
International Journal of Gynecological Pathology : Official Journal of the International Society of Gynecological Pathologists|April 25, 2024
Endometrial Cancer in a Family With RAD51D Gene MutationBrittany Gilmore, Linda Logan, Wendy McKinnon, et al.
Journal of the Association of Genetic Technologists|September 5, 2020
Acute Myeloid Leukemia with t(8;16)(p11.2;p13.3)/ KAT6A-CREBBP in a Patient with an NF1 Germline Mutation and Clinical Presentation Mimicking Acute Promyelocytic LeukemiaLiam Donnelly, Casey Rankins, Ximena Jordan Bruno, et al.
Human Pathology|October 25, 2011
Colonic ganglioneuromatous polyposis and metastatic adenocarcinoma in the setting of Cowden syndrome: a case report and literature reviewJoshua W Trufant, Laura Greene, Deborah L Cook, et al.
International Journal of Gynecological Pathology : Official Journal of the International Society of Gynecological Pathologists|February 12, 2022
Serous Tubal Intraepithelial Carcinoma in a Risk-reducing Salpingo-oophorectomy Specimen From a RAD51D Mutation Carrier: A Case ReportKalin J Gregory-Davis, Allison Walker, Laura S Colello, et al.
Journal of Cutaneous Pathology|December 14, 2011
Familial multiple pilomatrixomas as a presentation of attenuated adenomatosis polyposis coliJoshua Trufant, Wayne Kurz, Amylynne Frankel, et al.
Familial Cancer|May 26, 2009
Survey of unaffected BRCA and mismatch repair (MMR) mutation positive individualsWendy McKinnon, Kimberly C Banks, Joan Skelly, et al.
Human Mutation|April 23, 2002
A HOXA13 allele with a missense mutation in the homeobox and a dinucleotide deletion in the promoter underlies Guttmacher syndromeJeffrey W Innis, Frances R Goodman, Chiara Bacchelli, et al.
Psycho-Oncology|May 20, 2014
Intentions for risk-reducing surgery among high-risk women referred for BRCA1/BRCA2 genetic counselingAngie Tong, Scott Kelly, Rachel Nusbaum, et al.
Pageof 3