Next Generation Sequencing Analysis of Congenital Hypothyroidism Patients in A Single Tertiary Center

被引:0
|
作者
Park, Jisun [1 ,2 ]
Kim, Sujin [1 ]
Lee, Jieun [1 ]
机构
[1] Inha Univ Hosp, Incheon, South Korea
[2] Songdo Miso Childrens Hosp, Incheon, South Korea
来源
HORMONE RESEARCH IN PAEDIATRICS | 2022年 / 95卷 / SUPPL 2期
关键词
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
P1-388
引用
收藏
页码:412 / 412
页数:1
相关论文
共 50 条
  • [1] Next-generation sequencing analysis of twelve known causative genes in congenital hypothyroidism
    Fan, Xin
    Fu, Chunyun
    Shen, Yiping
    Li, Chuan
    Luo, Shiyu
    Li, Qifei
    Luo, Jingsi
    Su, Jiasun
    Zhang, Shujie
    Hu, Xuyun
    Chen, Rongyu
    Gu, Xuefan
    Chen, Shaoke
    CLINICA CHIMICA ACTA, 2017, 468 : 76 - 80
  • [2] Analysis of hypothyroidism NGS test in Korean patients with congenital hypothyroidism in a single center
    Jung, So Yoon
    Lee, Jeongho
    HORMONE RESEARCH IN PAEDIATRICS, 2021, 94 (SUPPL 1): : 172 - 173
  • [3] Genetic etiology in patients diagnosed with congenital hypothyroidism with new-generation sequencing: A single-center experience
    Kaplan, Emel Hatun Aytac
    Mermer, Serdar
    ARCHIVES DE PEDIATRIE, 2024, 31 (06): : 374 - 379
  • [4] Next-generation sequencing analysis of TSHR in 384 Chinese subclinical congenital hypothyroidism (CH) and CH patients
    Fu, Chunyun
    Wang, Jin
    Luo, Shiyu
    Yang, Qi
    Li, Qifei
    Zheng, Haiyang
    Hu, Xuyun
    Su, Jiasun
    Zhang, Shujie
    Chen, Rongyu
    Luo, Jingsi
    Zhang, Yue
    Shen, Yiping
    Wei, Hongwei
    Meng, Dahua
    Gui, Baoheng
    Zeng, Zhangqin
    Fan, Xin
    Chen, Shaoke
    CLINICA CHIMICA ACTA, 2016, 462 : 127 - 132
  • [5] Genetic spectrum of 26 Korean patients with congenital hypothyroidism by targeted next-generation sequencing
    Oh, Arum
    Han, Heon-Seok
    HORMONE RESEARCH IN PAEDIATRICS, 2022, 95 (SUPPL 2): : 405 - 405
  • [6] Targeted next-generation sequencing of thirteen causative genes in Chinese patients with congenital hypothyroidism
    Long, Wei
    Lu, Guanting
    Zhou, Wenbai
    Yang, Yugi
    Zhang, Bin
    Zhou, Hong
    Jiang, Lihua
    Yu, Bin
    ENDOCRINE JOURNAL, 2018, 65 (10) : 1019 - 1028
  • [7] Next-Generation Sequencing for Patients with Sarcoma: A Single Center Experience
    Cote, Gregory M.
    He, Jie
    Choy, Edwin
    ONCOLOGIST, 2018, 23 (02): : 234 - 242
  • [8] Identification of Novel Fusions in Melanoma by Next-Generation Sequencing: A Retrospective Analysis of 144 Patients from a Single Tertiary Cancer Center
    Kim, Moon Joo
    Yang, Richard
    Nagarajan, Priya
    Aung, Phyu
    Curry, Jonathan
    Cho, Woo Cheal
    LABORATORY INVESTIGATION, 2024, 104 (03) : S531 - S533
  • [9] Genotype analysis by next generation sequencing in severe FXI deficiency patients: A single center experience
    Riccardi, F.
    Quintavalle, G.
    Matichecchia, A.
    Coppola, A.
    Rivolta, G. F.
    Tagliaferri, A.
    HAEMOPHILIA, 2019, 25 : 88 - 88
  • [10] Screening of frequent variants associated with congenital hypothyroidism: a comparison with next generation sequencing
    Watanabe, Daisuke
    Yagasaki, Hideaki
    Narusawa, Hiromune
    Saito, Tomohiro
    Mitsui, Yumiko
    Miyake, Kunio
    Ohta, Masanori
    Inukai, Takeshi
    ENDOCRINE JOURNAL, 2021, 68 (12) : 1411 - 1419