Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: Glioma and PMS2[original query] |
---|
Hereditary brain tumor with a homozygous germline mutation in PMS2: pedigree analysis and prenatal screening in a family with constitutional mismatch repair deficiency (CMMRD) syndrome. Familial cancer 2018 11 18 (2): 261-265. Baig Shahid Mahmood, Fatima Ambrin, Tariq Muhammad, Khan Tahir Naeem, Ali Zafar, Faheem Mohammad, Mahmood Humera, Killela Patrick, Waitkus Matthew, He Yiping, Zhao Fangping, Wang Sizhen, Jiao Yuchen, Yan H |
Sporadic and Lynch syndrome-associated mismatch repair-deficient brain tumors. Laboratory investigation; a journal of technical methods and pathology 2021 12 102 (2): 160-171. Kim Hyunhee, Lim Ka Young, Park Jin Woo, Kang Jeongwan, Won Jae Kyung, Lee Kwanghoon, Shim Yumi, Park Chul-Kee, Kim Seung-Ki, Choi Seung-Hong, Kim Tae Min, Yun Hongseok, Park Sung-H |
Comprehensive profiling of pathogenic germline large genomic rearrangements in a pan-cancer analysis. Molecular oncology 2023 4 . Sun Zhe, Bai Chujie, Su Miaoyi, Tang Haimeng, Wu Xiaoying, Wang Yue, Bao Hua, Liu Xunbiao, Wu Xue, Shao Yang, Xu B |
Sporadic and Lynch syndrome-associated mismatch repair-deficient brain tumors. Laboratory investigation; a journal of technical methods and pathology 2023 2 102 (2): 160-171. Kim Hyunhee, Lim Ka Young, Park Jin Woo, Kang Jeongwan, Won Jae Kyung, Lee Kwanghoon, Shim Yumi, Park Chul-Kee, Kim Seung-Ki, Choi Seung-Hong, Kim Tae Min, Yun Hongseok, Park Sung-H |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 22, 2024
- Content source: