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

Document Type

Article

Author

Fadra, N.; Schultz-Rogers, L.E.; Chanana, P.; Cousin, M.A.; Macke, E.L.; Ferrer, A.; Pinto e Vairo, F.; Olson, R.J.; Oliver, G.R.; Mulvihill, L.A.; Jenkinson, G.; Klee, E.W.

Source

In: BMC Genomics. (BMC Genomics, December 2024, 25(1))

Subject

Language

English

ISSN

14712164

Online Access

Full Text (ProQuest Central) Full Text (Gale Academic Onefile) Open Access (BioMed Central) Open Access (EBSCO) Web of Science JCR 저널정보 Scopus Find it@PNU

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