Hereditary Predisposition to Oncological Diseases in Russian Pediatric Patients as Revealed by Clinical Exome Sequencing

Nasedkina T.; Lisitsa T.; Shumilova S.; Zhukovskaya E.; Kasatkin V.; Karelin A.

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Hereditary Predisposition to Oncological Diseases in Russian Pediatric Patients as Revealed by Clinical Exome Sequencing

机译：临床外壳测序揭示的俄罗斯小儿患者肿瘤疾病的遗传性易感性

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来源
《Pediatric blood & cancer》 |2019年第s4期|共1页
作者
Nasedkina T.; Lisitsa T.; Shumilova S.; Zhukovskaya E.; Kasatkin V.; Karelin A.;
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作者单位

Dmitry Rogachev Natl Res Ctr Pediat Hematol Oncol Clin Rehabil Res Ctr Patients Remiss Russkoye;

Dmitry Rogachev Natl Res Ctr Pediat Hematol Oncol Clin Rehabil Res Ctr Patients Remiss Russkoye;

Russian Acad Sci Engelhardt Inst Mol Biol Lab Biol Microchips Moscow Russia;

Dmitry Rogachev Natl Res Ctr Pediat Hematol Oncol Clin Rehabil Res Ctr Patients Remiss Russkoye;

Dmitry Rogachev Natl Res Ctr Pediat Hematol Oncol Clin Rehabil Res Ctr Patients Remiss Russkoye;

Dmitry Rogachev Natl Res Ctr Pediat Hematol Oncol Clin Rehabil Res Ctr Patients Remiss Russkoye;

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正文语种 eng
中图分类儿科学;
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1. Hereditary Predisposition to Oncological Diseases in Russian Pediatric Patients as Revealed by Clinical Exome Sequencing [J] . Nasedkina T., Lisitsa T., Shumilova S., Pediatric blood & cancer . 2019,第S4期

机译：临床外壳测序揭示的俄罗斯小儿患者肿瘤疾病的遗传性易感性
2. Whole‐exome sequencing of sickle cell disease patients with hyperhemolysis syndrome suggests a role for rare variation in disease predisposition [J] . Mwesigwa Savannah, Moulds Joann M., Chen Alice, Transfusion: The Journal of the American Association of Blood Banks . 2018,第3期

机译：镰状细胞病患者的全外膜测序患者的高速溶性综合征表明疾病易感性罕见变异的作用
3. Integrative Genetic and Clinical Analysis through Whole Exome Sequencing in 1001 Diffuse Large B Cell Lymphoma (DLBCL) Patients Reveals Novel Disease Drivers and Risk Groups [J] . Zhang Jenny, Reddy Anupama, Love Cassandra, Blood: The Journal of the American Society of Hematology . 2016,第22期

机译：通过全面exome测序在1001弥漫性大B细胞淋巴瘤（DLBCL）患者中的整合遗传和临床分析揭示了新型疾病驱动因素和风险群体
4. FOCUS ON HEREDITARY DISEASES GENETIC PREDISPOSITIONS CLINICAL LABORATORY DIAGNOSTIC APPROACH TO HEREDITARY DISEASES [C] . anonymous American College of Veterinary Internal Medicine Forum . 2008

机译：专注于遗传性疾病与遗传易感性临床和实验室诊断方法对遗传性疾病
5. Discovery of novel genes that cause rare pediatric renal diseases using whole-exome sequencing [D] . Lemaire, Mathieu. 2015

机译：使用全基因组测序发现导致罕见的小儿肾脏疾病的新基因
6. TBIO-20. CLINICAL TUMOR WHOLE EXOME SEQUENCING FOR PEDIATRIC NEURO-ONCOLOGY PATIENTS – RESULTS FROM THE BAYLOR ADVANCING SEQUENCING IN CHILDHOOD CANCER CARE (BASIC3) CLINICAL SEQUENCING STUDY [O] . Frank Lin, Samara Potter, Michelle Ting, 2018

机译：TBIO-20。小儿神经肿瘤患者的临床肿瘤全基因组测序-儿童癌症护理（BASIC3）临床测序研究中Baylor先进测序的结果
7. An Ophthalmic Targeted Exome Sequencing Panel as a Powerful Tool to Identify Causative Mutations in Patients Suspected of Hereditary Eye Diseases [O] . Panfeng Wang, Shiqiang Li, Wenming Sun, 2019

机译：一种眼科靶向外壳测序面板作为鉴定患有遗传性眼病患者的致病性突变的强大工具

Hereditary Predisposition to Oncological Diseases in Russian Pediatric Patients as Revealed by Clinical Exome Sequencing

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