S-EPMC11982971 - Clinically relevant variants detected in Chinese children with global developmental delay/intellectual disability: An exome-wide sequencing study. - OmicsDI

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Clinically relevant variants detected in Chinese children with global developmental delay/intellectual disability: An exome-wide sequencing study.

ABSTRACT:

SUBMITTER: Qiao Y

PROVIDER: S-EPMC11982971 | biostudies-literature | 2025 Jul

REPOSITORIES: biostudies-literature