IDENTIFICATION OF TARGETABLE MUTATIONS IN RARE PEDIATRIC BRAIN TUMORS BY CLINICAL WHOLE EXOME SEQUENCING

被引：0

作者：

Lin, Frank Y. ^{[1
]}

Bavle, Abhishek ^{[1
]}

Wheeler, David ^{[1
]}

Gibbs, Richard ^{[1
]}

Lam, Sandi ^{[1
]}

Su, Jack ^{[1
]}

Chintagumpala, Murali ^{[1
]}

Adesina, Adekunle ^{[1
]}

Roy, Angshumoy ^{[1
]}

Plon, Sharon E. ^{[1
]}

Parsons, D. Williams ^{[1
]}

机构：

[1] Texas Childrens Hosp, Baylor Coll Med, Texas Childrens Canc Ctr, Houston, TX 77030 USA

来源：

NEURO-ONCOLOGY | 2015年 / 17卷

关键词：

D O I：

暂无

中图分类号：

R73 [肿瘤学];

学科分类号：

100214 ;

摘要：

GE-06

引用

页码：8 / 8

页数：1

共 50 条

[31] Whole exome sequencing in the pediatric neuromuscular clinic
Meyer, A.
Cottrell, C.
Reshmi, S.
Pfau, R.
Lee, K.
Mathew, M.
Corsmeier, D.
Jayaraman, V.
Dave-Wala, A.
Hashimoto, S.
Matthews, T.
Mouhlas, D.
Stein, M.
Waldrop, M.
Flanigan, K.
NEUROMUSCULAR DISORDERS, 2020, 30 : S142 - S142
[32] Whole Exome Sequencing in unsolved pediatric cases
Moresco, G.
Rondinone, O.
Mauri, A.
Santaniello, C.
Costanza, J.
Rinaldi, B.
Rosina, E.
Colapietro, P.
Tabano, S.
Fontana, L.
Milani, D.
Miozzo, M.
EUROPEAN JOURNAL OF HUMAN GENETICS, 2020, 28 (SUPPL 1) : 933 - 933
[33] The Clinical Utility of Clinical Whole Exome Sequencing
Tumer, S. A.
Steinmetz, H. B.
Dinulos, M. P.
Moeschler, J. B.
Vallee, S. E.
Upton, S. J.
Tafe, L. J.
Chen, R.
Garcia, S.
Church, D.
Tirch, J.
Huang, A.
Lefferts, J. A.
Tsongalis, G. J.
JOURNAL OF MOLECULAR DIAGNOSTICS, 2014, 16 (06): : 706 - 706
[34] Targetable Fusion Genes in Pediatric Brain Tumors
Nakano, Yoshiko
Hirato, Junko
Kurozumi, Kazuhiko
Date, Isao
Tusubuchi, Takao
Yamamoto, Tetsuya
Matsumura, Akira
Sakamoto, Hiroaki
Ito, Jumpei
Shima, Haruko
Miwa, Tomoru
Kohno, Takashi
Kogure, Yasunori
Keisuke, Kataoka
Yoshioka, Takako
Hara, Junichi
Yoshida, Akihiko
Ichimura, Koichi
PEDIATRIC BLOOD & CANCER, 2019, 66 : S7 - S8
[35] Results of whole-exome sequencing of germline DNA in pediatric patients with solid tumors
Drabova, Klara
Pokorna, Petra
Palova, Hana
Adamcova, Sona
Bystry, Vojtech
Jugas, Robin
Slaby, Ondrej
Sterba, Jaroslav
EUROPEAN JOURNAL OF HUMAN GENETICS, 2024, 32 : 556 - 556
[36] Clinical or whole exome sequencing for mutation analysis in families with rare genetic syndromes?
Paszekova, Helena
Hruskova, Lucie
Pis, Tomas
Vlckova, Zdenka
Michalovska, Renata
EUROPEAN JOURNAL OF HUMAN GENETICS, 2023, 31 : 221 - 221
[37] Clinical Application of Whole Exome Sequencing to Identify Rare but Remediable Neurologic Disorders
Kim, Min-Jee
Yum, Mi-Sun
Seo, Go Hun
Lee, Yena
Jang, Han Na
Ko, Tae-Sung
Lee, Beom Hee
JOURNAL OF CLINICAL MEDICINE, 2020, 9 (11) : 1 - 14
[38] Identification of germline and somatic mutations in pancreatic adenosquamous carcinoma using whole exome sequencing
Ma, Hongyun
Song, Bin
Guo, Shiwei
Li, Gang
Jin, Gang
CANCER BIOMARKERS, 2020, 27 (03) : 389 - 397
[39] Identification of novel mutations in preaxial polydactyly patients through whole-exome sequencing
Wang, Tao
Xuan, Zhaopeng
Dou, Yichen
Liu, Yang
Fu, Yanyan
Ren, Jingyan
Lu, Laijin
MOLECULAR GENETICS & GENOMIC MEDICINE, 2019, 7 (06):
[40] Identification of Germline Mutations in Young Never Smokers With Lung Adenocarcinoma by Whole Exome Sequencing
Zhang, Y.
Fu, F.
Chen, H.
JOURNAL OF THORACIC ONCOLOGY, 2021, 16 (10) : S1211 - S1211

← 1 2 3 4 5 →