S-EPMC11020449 - Identification of skewed X chromosome inactivation using exome and transcriptome sequencing in patients with suspected rare genetic disease - OmicsDI

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Identification of skewed X chromosome inactivation using exome and transcriptome sequencing in patients with suspected rare genetic disease

ABSTRACT:

SUBMITTER: Fadra N

PROVIDER: S-EPMC11020449 | biostudies-literature | 2024 Jan

REPOSITORIES: biostudies-literature