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International Journal of Developmental Neuroscience : the Official Journal of the International Society for Developmental Neuroscience
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April 23, 2026
Autism Spectrum Disorder Caused by a Novel De Novo SCN2A Mutation: A Case Report
Jinghan Gao, Wenmiao Liu, Yucui Zang, et al.
Seizure
|
May 10, 2026
Genetic characterization of DDX11 variants identified in a Chinese family with Warsaw breakage syndrome
Xue Zhong, Wenmiao Liu, Xueping Zheng, et al.
Pregnancy Hypertension
|
July 3, 2024
Association of NLRP3 and IL-4 VNTR polymorphisms and genetic susceptibility to preeclampsia: A case-control study
Mingxuan Che, Yinglei Xu, Yucui Zang, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics
|
October 2, 2022
[Analysis of genetic variant in a patient with juvenile meterochromic leukodystrophy]
Xiao Zhang, Miaomiao Li, Jianhua Ma, et al.
BMC Pregnancy and Childbirth
|
November 22, 2021
Association between polymorphisms rs2228001 and rs2228000 in XPC and genetic susceptibility to preeclampsia: a case control study
Jingli Wang, Chengcheng Guan, Jing Sui, et al.
Frontiers in Endocrinology
|
May 20, 2020
<i>DUOX2</i> and <i>DUOXA2</i> Variants Confer Susceptibility to Thyroid Dysgenesis and Gland-<i>in-situ</i> With Congenital Hypothyroidism
Fengqi Wang, Yucui Zang, Miaomiao Li, et al.
The Analyst
|
May 9, 2013
A colorimetric method for H1N1 DNA detection using rolling circle amplification
Yasi Xing, Ping Wang, Yucui Zang, et al.
Endokrynologia Polska
|
February 26, 2020
Genetic testing of PAX8 mutations associated with thyroid dysgenesis in Chinese congenital hypothyroidism patients
Miaomiao Li, Fang Wang, Xiuli Wang, et al.
Journal of Cellular Biochemistry
|
August 4, 2018
Novel THRB mutation analysis in congenital hypothyroidism with thyroid dysgenesis
Zhixia Zhou, Chengyu Yang, Fuyan Lv, et al.
Frontiers in Endocrinology
|
August 21, 2019
Identification of Two Missense Mutations in <i>DUOX1</i> (p.R1307Q) and <i>DUOXA1</i> (p.R56W) That Can Cause Congenital Hypothyroidism Through Impairing H<sub>2</sub>O<sub>2</sub> Generation
Shiguo Liu, Wenxiu Han, Yucui Zang, et al.
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Search research articles
Search
Showing results (1-10 of 11) with videos related to
Sort By:
Page
of 2
International Journal of Developmental Neuroscience : the Official Journal of the International Society for Developmental Neuroscience
|
April 23, 2026
Autism Spectrum Disorder Caused by a Novel De Novo SCN2A Mutation: A Case Report
Jinghan Gao, Wenmiao Liu, Yucui Zang, et al.
Seizure
|
May 10, 2026
Genetic characterization of DDX11 variants identified in a Chinese family with Warsaw breakage syndrome
Xue Zhong, Wenmiao Liu, Xueping Zheng, et al.
Pregnancy Hypertension
|
July 3, 2024
Association of NLRP3 and IL-4 VNTR polymorphisms and genetic susceptibility to preeclampsia: A case-control study
Mingxuan Che, Yinglei Xu, Yucui Zang, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics
|
October 2, 2022
[Analysis of genetic variant in a patient with juvenile meterochromic leukodystrophy]
Xiao Zhang, Miaomiao Li, Jianhua Ma, et al.
BMC Pregnancy and Childbirth
|
November 22, 2021
Association between polymorphisms rs2228001 and rs2228000 in XPC and genetic susceptibility to preeclampsia: a case control study
Jingli Wang, Chengcheng Guan, Jing Sui, et al.
Frontiers in Endocrinology
|
May 20, 2020
<i>DUOX2</i> and <i>DUOXA2</i> Variants Confer Susceptibility to Thyroid Dysgenesis and Gland-<i>in-situ</i> With Congenital Hypothyroidism
Fengqi Wang, Yucui Zang, Miaomiao Li, et al.
The Analyst
|
May 9, 2013
A colorimetric method for H1N1 DNA detection using rolling circle amplification
Yasi Xing, Ping Wang, Yucui Zang, et al.
Endokrynologia Polska
|
February 26, 2020
Genetic testing of PAX8 mutations associated with thyroid dysgenesis in Chinese congenital hypothyroidism patients
Miaomiao Li, Fang Wang, Xiuli Wang, et al.
Journal of Cellular Biochemistry
|
August 4, 2018
Novel THRB mutation analysis in congenital hypothyroidism with thyroid dysgenesis
Zhixia Zhou, Chengyu Yang, Fuyan Lv, et al.
Frontiers in Endocrinology
|
August 21, 2019
Identification of Two Missense Mutations in <i>DUOX1</i> (p.R1307Q) and <i>DUOXA1</i> (p.R56W) That Can Cause Congenital Hypothyroidism Through Impairing H<sub>2</sub>O<sub>2</sub> Generation
Shiguo Liu, Wenxiu Han, Yucui Zang, et al.
Page
of 2