Identification of a novel phenotype of external ear deformity related to Coffin–Siris syndrome‐9 and literature review
R Wu, W Tang, P Li, Z Meng, X Li… - American Journal of … - Wiley Online Library
De novo germline variants of the SRY‐related HMG‐box 11 gene (SOX11) have been
reported to cause Coffin–Siris syndrome‐9 (CSS‐9), a rare congenital disorder associated …
reported to cause Coffin–Siris syndrome‐9 (CSS‐9), a rare congenital disorder associated …
Identification of a novel phenotype of external ear deformity related to Coffin-Siris syndrome-9 and literature review
R Wu, W Tang, P Li, Z Meng, X Li… - American journal of … - pubmed.ncbi.nlm.nih.gov
De novo germline variants of the SRY-related HMG-box 11 gene (SOX11) have been
reported to cause Coffin-Siris syndrome-9 (CSS-9), a rare congenital disorder associated …
reported to cause Coffin-Siris syndrome-9 (CSS-9), a rare congenital disorder associated …
Identification of a novel phenotype of external ear deformity related to Coffin-Siris syndrome-9 and literature review.
R Wu, W Tang, P Li, Z Meng, X Li… - American Journal of …, 2024 - europepmc.org
De novo germline variants of the SRY-related HMG-box 11 gene (SOX11) have been
reported to cause Coffin-Siris syndrome-9 (CSS-9), a rare congenital disorder associated …
reported to cause Coffin-Siris syndrome-9 (CSS-9), a rare congenital disorder associated …