Subtelomeric Deletions of Chromosome 6P: Molecular and Cytogenetic Characterization of Three New Cases with Phenotypic Overlap with Ritscher-Schinzel (3C) Syndrome
AuthID
P-000-3WV
P-000-3WV
© 2025 CRACS & Inesc TEC - All Rights Reserved Política de Privacidade | Terms of Service