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Temporal order of RNase IIIb and loss-of-function mutations during development determines phenotype in pleuropulmonary blastoma / DICER1 syndrome: a unique variant of the two-hit tumor suppression model

机译：RNase IIIB的时间顺序和开发过程中的功能丧失突变决定了胸膜尿瘤/ DICER1综合征中的表型：双击肿瘤抑制模型的独特变体

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Mark Brenneman; Amanda Field; Jiandong Yang; Gretchen Williams; Leslie Doros; Christopher Rossi; Kris Ann Schultz; Avi Rosenberg; Jennifer Ivanovich; Joyce Turner; Heather Gordish-Dressman; Douglas Stewart; Weiying Yu; Anne Harris; Peter Schoettler; Paul Goodfellow; Louis Dehner; Yoav Messinger; D. Ashley Hill;
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1. Identification of somatic and germ-line DICER1 mutations in pleuropulmonary blastoma, cystic nephroma and rhabdomyosarcoma tumors within a DICER1 syndrome pedigree [J] . Lorena Fernández-Martínez, José Antonio Villegas, í?igo Santamaría, BMC Cancer . 2017,第1期

机译：在DICER1综合征谱系内鉴定胸膜肺母细胞瘤，囊性肾瘤和横纹肌肉瘤中的体细胞和种系DICER1突变
2. Ovarian sex cord-stromal tumors, pleuropulmonary blastoma and DICER1 mutations: a report from the International Pleuropulmonary Blastoma Registry. [J] . Schultz KA, Pacheco MC, Yang J, Gynecologic Oncology: An International Journal . 2011,第2期

机译：卵巢性索间质肿瘤，胸膜肺母细胞瘤和DICER1突变：国际胸膜肺母细胞瘤登记处的报告。
3. Expanding the phenotype of mutations in DICER1: Mosaic missense mutations in the RNase IIIb domain of DICER1 cause GLOW syndrome [J] . KleinS., LeeH., GhahremaniS., Journal of Medical Genetics . 2014,第5期

机译：扩大DICER1中突变的表型：DICER1 RNase IIIb域中的马赛克错义突变导致GLOW综合征
4. Temporal order of RNase IIIb and loss-of-function mutations during development determines phenotype in pleuropulmonary blastoma /DICER1 syndrome: a unique variant of the two-hit tumor suppression model [O] . Mark Brenneman, Amanda Field, Jiandong Yang, -1

机译：RNase IIIb的时间顺序和发育过程中功能丧失的突变决定了胸膜肺母细胞瘤的表型/DICER1综合征：两次打击肿瘤抑制模型的独特变体
5. Identification of somatic and germ-line DICER1 mutations in pleuropulmonary blastoma, cystic nephroma and rhabdomyosarcoma tumors within a DICER1 syndrome pedigree [O] . 2017

机译：在DICER1综合征谱系中鉴定胸膜肺母细胞瘤，囊性肾瘤和横纹肌肉瘤中的体细胞和种系DICER1突变

Temporal order of RNase IIIb and loss-of-function mutations during development determines phenotype in pleuropulmonary blastoma / DICER1 syndrome: a unique variant of the two-hit tumor suppression model

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