Next-generation sequencing of NKX2.1 , FOXE1 , PAX8 , NKX2.5 , and TSHR in 100 Chinese patients with congenital hypothyroidism and athyreosis-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Next-generation sequencing of NKX2.1 , FOXE1 , PAX8 , NKX2.5 , and TSHR in 100 Chinese patients with congenital hypothyroidism and athyreosis

Published:2017-07 Issue: Volume:470 Page:36-41
ISSN:0009-8981
Container-title:Clinica Chimica Acta
language:en
Short-container-title:Clinica Chimica Acta

Author:

Wang Fang,Liu Chang,Jia Xiuhua,Liu Xiangju,Xu Yinglei,Yan Shengli,Jia Xuewen,Huang Zuzhou,Liu Shiguo,Gu Maosheng

Funder

National Natural Science Foundation of China

Shandong Provincial Population and Family Planning Commission

Publisher

Elsevier BV

Subject

Biochemistry (medical),Clinical Biochemistry,Biochemistry,General Medicine

Reference29 articles.

1. Congenital hypothyroidism in neonates;Anjum;Indian J. Endocr. Metab.,2014

2. Prevalence and etiology of congenital hypothyroidism detected through an argentine neonatal screening program (1997–2010);Chiesa;Horm. Res. Paediatr.,2013

3. Thyroid dysfunctions in children detected in mass screening for congenital hypothyroidism;Kumorowicz-Czoch;J. Pediatr. Endocrinol. Metab.,2011

4. Genetics of normal and abnormal thyroid development in humans;Szinnai;Best Pract. Res. Clin. Endocrinol. Metab.,2014

5. Thyroid developmental anomalies in first degree relatives of children with congenital hypothyroidism;Leger;J. Clin. Endocrinol. Metab.,2002

Cited by 22 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Revealing the genetic complexity of hypothyroidism: integrating complementary association methods;Frontiers in Genetics;2024-06-11

2. Identification of Eukaryotic Translation Initiation Factor 4B as a Novel Candidate Gene for Congenital Hypothyroidism;The Journal of Clinical Endocrinology & Metabolism;2024-04-24

3. Can inactivation mutation in the thyroid stimulating hormone receptor gene and hyperthyroidism coexist?: A case report;Medicine;2024-01-19

4. Functional Insights into Hypothyroidism Etiology through Complementary Genetic Association Methods;2023-11-29

5. Use of whole exome sequencing for identification of genetic variants related to Growth Hormone Deficiency and Short Stature: A Family-Based Study;Pakistan Journal of Medical Sciences;2023-07-11

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线，采集、加工和组织学术论文而形成的新型学术文献查询和分析系统，可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容，当前同舟云学术共收录了国内外主流学术期刊6万余种，收集的期刊论文及会议论文总量共计约1.5亿篇，并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询！咨询电话：010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号京ICP备18003416号-3