Associated Papers
Novel FOXP2 variant associated with speech and language dysfunction in a Chinese family and literature review.
Che F et al.
Journal of Applied Genetics, 2024
Whole-exome sequencing in syndromic craniosynostosis increases diagnostic yield and identifies candidate genes in osteogenic signaling pathways.
Tønne E et al.
American Journal of Medical Genetics. Part A, 2022
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