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Biallelic variants in MESD, which encodes a WNT-signaling-related protein, in four new families with recessively inherited osteogenesis imperfecta

Document Type

Article

Author

Tran, T.T.; Byers, P.H.; Keller, R.B.; Pepin, M.; Guillemyn, B.; Malfait, F.; Symoens, S.; Coucke, P.; Corteville, J.E.; Khatib, S.; Bagherian, H.; Fallah, M.-S.; Zeinali, S.; Witters, P.; Levtchenko, E.; Nickerson, D.A.; Bamshad, M.J.; Chong, J.X.

Source

In: Human Genetics and Genomics Advances. (Human Genetics and Genomics Advances, 14 October 2021, 2(4))

Subject

Language

English

ISSN

26662477

Online Access

Full Text (ScienceDirect 종량제) Full Text (Clinical Key) Full Text (ScienceDirect O/A) Scopus Find it@PNU

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