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Clinical features associated with CTNNB1 de novo loss of function mutations in ten individuals

Document Type

Article

Author

Kharbanda, Mira; Pilz, Daniela T.; Tomkins, Susan; Chandler, Kate; Saggar, Anand; Fryer, Alan; McKay, Victoria; Louro, Pedro; Smith, Jill Clayton; Burn, John; Kini, Usha; De Burca, Anna; FitzPatrick, David R.; Kinning, Esther

Source

In European Journal of Medical Genetics February 2017 60(2):130-135

Subject

Language

ISSN

1769-7212

Online Access

Full Text (ScienceDirect 종량제) Full Text (Clinical Key) Web of Science JCR 저널정보 Scopus Find it@PNU

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