학술논문

A non-coding insertional mutation of Grhl2 causes gene over-expression and multiple structural anomalies including cleft palate, spina bifida and encephalocele

Document Type

Article

Author

Crane-Smith, Z.; De Castro, S.C.P.; Nikolopoulou, E.; Mather, E.; Santos, C.; Copp, A.J.; Greene, N.D.E.; Wolujewicz, P.; Ross, M.E.; Smedley, D.; Lei, Y.; Finnell, R.H.; Hopkinson, M.; Pitsillides, A.A.

Source

In: Human Molecular Genetics. (Human Molecular Genetics, 1 September 2023, 32(17):2681-2692)

Subject

Language

English

ISSN

14602083
09646906

Online Access

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

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