Associated Papers
Rare variants in NRSN2 cause non-syndromic orofacial cleft through dysregulation of TGF-β signaling.
Zheng X et al.
Genes & Diseases, 2026
41624910 (PubMed )
Supplement: mmc2.docx
Genomic origin and intratumor heterogeneity revealed by sequencing on carcinomatous and sarcomatous components of pulmonary sarcomatoid carcinoma.
Liu X et al.
Oncogene, 2021
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