Associated Papers
Identification of the genetic basis of sporadic polydactyly in China by targeted sequencing.
Zu B et al.
Computational and Structural Biotechnology Journal, 2021
34194672 (PubMed )
Supplement: mmc1.xlsx › S3
Thyroid cancers of follicular origin in a genomic light: in-depth overview of common and unique molecular marker candidates.
Pstrąg N et al.
Molecular Cancer, 2018
The genetic characteristics of congenital hypothyroidism in China by comprehensive screening of 21 candidate genes.
Sun F et al.
European Journal of Endocrinology, 2018
29650690 (PubMed )
Supplement: eje-178-623-t001.pdf
Somatic Mutations of FOXE1 in Papillary Thyroid Cancer.
Mond M et al.
Thyroid : Official Journal of the American Thyroid Association, 2015
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