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A syndromic form of Pierre Robin sequence is caused by 5q23 deletions encompassing FBN2 and PHAX

Document Type

Article

Author

Ansari, Morad; Rainger, Jacqueline K.; Murray, Jennie E.; Hanson, Isabel; Firth, Helen V.; Mehendale, Felicity; Amiel, Jeanne; Gordon, Christopher T.; Percesepe, Antonio; Mazzanti, Laura; Fryer, Alan; Ferrari, Paola; Devriendt, Koenraad; Temple, I. Karen; FitzPatrick, David R.

Source

In European Journal of Medical Genetics October 2014 57(10):587-595

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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