Uncovering potential causal genes for undiagnosed congenital anomalies using an in-house pipeline for trio-based whole-genome sequencing.Published in:Human Genomics, 2025, v. 1, p. 1, doi. 10.1186/s40246-024-00709-2By:Kim, Jeong-Min;Cho, Hye-Won;Shin, Dong Mun;Kim, Oc-Hee;Kim, Jihyun;Lee, Hyeji;Lee, Gang-Hee;An, Joon-Yong;Yang, Misun;Jo, Heui Seung;Jang, Ja-Hyun;Chang, Yun Sil;Park, Hyun-Young;Park, Mi-HyunPublication type:Article