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Functional genomics analysis identifies loss of HNF1B function as a cause of Mayer-Rokitansky-Küster-Hauser syndrome

Document Type

Article

Author

Thomson, E.; Gopalakrishnan Bhaskaran, P.; Pelosi, E.; Tran, M.; Nguyen, Q.; Koopman, P.; Robevska, G.; Ayers, K.; van der Bergen, J.; Sinclair, A.; Haan, E.; Cereghini, S.; Vash-Margita, A.; Margetts, M.; Hensley, A.

Source

In: Human molecular genetics. (Human molecular genetics, 6 March 2023, 32(6):1032-1047)

Subject

Language

English

ISSN

14602083

Online Access

Full Text (Oxford University Press) Open Access (EBSCO) Web of Science JCR 저널정보 Scopus Find it@PNU

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