de Filippis et al., 2016 - JAG1 loss-of-function variations as a novel predisposing event in the pathogenesis of congenital thyroid defects. The Journal of clinical endocrinology and metabolism   101(3):861-70 Full text @ J. Clin. Endocrinol. Metab.
6 Genes / Markers
Marker Type Symbol Name
Gene jag1a jagged canonical Notch ligand 1a
Gene jag1b jagged canonical Notch ligand 1b
Gene nkx2.4b NK2 homeobox 4b
Gene slc5a5 solute carrier family 5 member 5
Gene tg thyroglobulin
Gene tshba thyroid stimulating hormone subunit beta a
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