Molecular and clinical characteristics of congenital hypothyroidism in a large cohort study based on comprehensive thyroid transcription factor mutation screening in Henan-Reference-Cited by-同舟云学术

Molecular and clinical characteristics of congenital hypothyroidism in a large cohort study based on comprehensive thyroid transcription factor mutation screening in Henan

Published:2021-07 Issue: Volume:518 Page:162-169
ISSN:0009-8981
Container-title:Clinica Chimica Acta
language:en
Short-container-title:Clinica Chimica Acta

Author:

Li Liangshan,Jia Chenlu,Li Xiaole,Wang Fang,Wang Yangang,Chen Yanping,Liu Shiguo,Zhao Dehua

Publisher

Elsevier BV

Subject

Biochemistry, medical,Clinical Biochemistry,Biochemistry,General Medicine

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1. Clinical, biochemical characteristics and genotype-phenotype analysis of congenital hypothyroidism diagnosed by newborn screening in China;Clinica Chimica Acta;2023-07

2. Effect of levothyroxine sodium on preterm infants with hypothyroidism;TROP J PHARM RES;2023

3. The Severity of Congenital Hypothyroidism With Gland-In-Situ Predicts Molecular Yield by Targeted Next-Generation Sequencing;The Journal of Clinical Endocrinology & Metabolism;2023-03-08

4. Novel Missense Variants in PAX8 and NKX2-1 Cause Congenital Hypothyroidism;International Journal of Molecular Sciences;2023-01-02

5. Mutation screening of eight genes and comparison of the clinical data in a Chinese cohort with congenital hypothyroidism;Endocrine;2022-09-20