Associated Papers
Multigene Detection Analysis of Multifocal Papillary Thyroid Carcinoma.
Fang X et al.
Clinical Endocrinology, 2025
Characteristics of germline DNA damage response gene mutations in ovarian cancer in Southwest China.
Fu K et al.
Scientific Reports, 2024
38509102 (PubMed )
Supplement: 41598_2024_52707_MOESM2_ESM.xlsx › mutation
The mutation screening in candidate genes related to thyroid dysgenesis by targeted next-generation sequencing panel in the Chinese congenital hypothyroidism.
Zhang RJ et al.
Clinical Endocrinology, 2022
Next-Generation Sequencing Enhances the Diagnosis Efficiency in Thyroid Nodules.
Tan LC et al.
Frontiers in Oncology, 2021
Targeted next-generation sequencing of thirteen causative genes in Chinese patients with congenital hypothyroidism.
Long W et al.
Endocrine Journal, 2018
Next-generation sequencing of NKX2.1, FOXE1, PAX8, NKX2.5, and TSHR in 100 Chinese patients with congenital hypothyroidism and athyreosis.
Wang F et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry, 2017
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