Showing results (791-800 of 1,519) with videos related to

Sort By:
Pageof 152
Familial Cancer|September 21, 2021
Outcomes of retesting in patients with previously uninformative cancer genetics evaluationsShenin A Sanoba, Erika S Koeppe, Michelle F Jacobs, et al.
Familial Cancer|July 22, 2023
Germline whole genome sequencing in adults with multiple primary tumorsYiming Wang, Qiliang Ding, Stephenie Prokopec, et al.
Familial Cancer|July 29, 2023
Prevalence and genetic spectrum associated with hereditary colorectal cancer syndromes, the need to improve cancer risk awareness, and family cascade testing in VietnamHuu-Thinh Nguyen, Y-Thanh Lu, Duc-Huy Tran, et al.
Familial Cancer|June 24, 2023
Mainstreamed genetic testing of breast cancer patients: experience from a single surgeon's practice in a large US Academic CenterTeresa S Chai, Kanhua Yin, Mackenzie Wooters, et al.
Familial Cancer|February 14, 2020
Co-occurrence of multiple endocrine neoplasia type 4 and spinal neurofibromatosis: a case reportPamela Brock, Jean Bustamante Alvarez, Amir Mortazavi, et al.
Familial Cancer|February 16, 2020
Mismatch repair gene pathogenic germline variants in a population-based cohort of breast cancerTu Nguyen-Dumont, Jason A Steen, Ingrid Winship, et al.
Familial Cancer|November 19, 2020
Early-onset malignant phyllodes breast tumor in a patient with germline pathogenic variants in NF1 and BRCA1 genesFrancesca Gensini, Roberta Sestini, Alessandro De Luca, et al.
Familial Cancer|November 20, 2020
Efficacy of paired tumor and germline testing in evaluation of patients with Lynch-like syndrome in a large integrated healthcare settingHolly Carwana, Elizabeth Hoodfar, JoAnn Bergoffen, et al.
Familial Cancer|September 23, 2020
Patient reported experiences following laparoscopic prophylactic bilateral salpingo-oophorectomy or salpingectomy in an ambulatory care hospitalRachel Trister, Michelle Jacobson, Patricia Nguyen, et al.
Familial Cancer|November 21, 2019
MLH1 promoter hypermethylation: are you absolutely sure about the absence of MLH1 germline mutation? About a new caseCaroline Kientz, Fabienne Prieur, Alix Clemenson, et al.
Pageof 152