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High Prevalence of Alterations in DNA Mismatch Repair Genes of Lynch Syndrome in Pediatric Patients with Adrenocortical Tumors Carrying a Germline Mutation on TP53

机译：儿科患者DNA综合征DNA错配修复基因的改变患病率高肾上腺导瘤TP53患者系列肿瘤

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Vania Balderrama Brondani; Luciana Montenegro; Amanda Meneses Ferreira Lacombe; Breno Marchiori Magalhães; Mirian Yumie Nishi; Mariana Ferreira de Assis Funari; Amanda de Moraes Narcizo; Lais Cavalca Cardoso; Sheila Aparecida Coelho Siqueira; Maria Claudia Nogueira Zerbini; Francisco Tibor Denes; Ana Claudia Latronico; Berenice Bilharinho Mendonca; Madson Queiroz Almeida; Antonio Marcondes Lerario; Ibere Cauduro Soares; Maria Candida Barisson Villares Fragoso;
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1. 中国乳腺癌患者循环肿瘤DNA中TP53突变的临床特征及预后价值 [J] . 易宗毕, 马飞, 荣国华, 癌症（英文版） . 2021,第005期
2. High Prevalence of Alterations in DNA Mismatch Repair Genes of Lynch Syndrome in Pediatric Patients with Adrenocortical Tumors Carrying a Germline Mutation on TP53 [J] . International journal of applied mechanics . 2020,第3期

机译：肾上腺皮质肿瘤肾上腺皮质肿瘤的林奇综合征DNA错配修复基因改变患病率高.TP53
3. SAT-155 High Prevalence Alterations on DNA Mismatch Repair Genes Related to Lynch Syndrome in Pediatric Patients with Adrenocortical Tumor Carried of the Germline Mutation on TP53 [J] . Brondani Vania Balderrama, Montenegro Luciana Ribeiro, Lacombe Amanda Meneses Ferreira, Journal of the Endocrine Society. . 2020,第Supplementa1期

机译：SAT-155在TP53对肾上腺皮质肿瘤的儿科患者中与林奇综合征有关的DNA错配修复基因的高流行改变。
4. Screening for germline mutations in mismatch repair genes in patients with Lynch syndrome by next generation sequencing [J] . Soares Barbara Luisa, Brant Ayslan Castro, Gomes Renan, Familial cancer . 2018,第3期

机译：下一代测序筛选林奇综合征患者失配修复基因中的种系突变
5. One germline mutation of PTCH gene in a Chinese family with non-syndromic keratocystic odontogenic tumours [C] . X. Wang, Y. Lu, G. Shen, Academic Committee Conference of Shanghai key lab of stomatology . 2011

机译：非综合征性角化囊性牙源性肿瘤的中国家庭中PTCH基因的一个种系突变
6. Evaluation of the accuracy of quantitative models in predicting Lynch syndrome (hereditary nonpolyposis colorectal cancer with defective DNA mismatch repair) mutations in a population-based sample of early-onset colorectal cancer patients [D] . Carpiniello, Lauren 2007

机译：在以人群为基础的早发性大肠癌患者样本中预测定量模型预测Lynch综合征（遗传性非息肉病性大肠直肠癌，DNA失配修复缺陷）的准确性
7. High Prevalence of Alterations in DNA Mismatch Repair Genes of Lynch Syndrome in Pediatric Patients with Adrenocortical Tumors Carrying a Germline Mutation on TP53 [O] . Vania Balderrama Brondani, Luciana Montenegro, Amanda Meneses Ferreira Lacombe, 2020

机译：小儿携带生殖细胞突变的TP53肾上腺皮质肿瘤患者Lynch综合征的DNA错配修复基因改变的高发生率
8. TumorNext-Lynch-MMR: a comprehensive next generation sequencing assay for the detection of germline and somatic mutations in genes associated with mismatch repair deficiency and Lynch syndrome [O] . Phillip N. Gray, Pei Tsai, Daniel Chen, 2018

机译：tumornext-lynch-mmr：一种综合的下一代测序测定，用于检测与错配修复缺陷和林奇综合征相关的基因中的种系和体细胞突变

High Prevalence of Alterations in DNA Mismatch Repair Genes of Lynch Syndrome in Pediatric Patients with Adrenocortical Tumors Carrying a Germline Mutation on TP53

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