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X-exome sequencing in Finnish families with Intellectual Disability - Four novel mutations and two novel syndromic phenotypes

Document Type

Article

Author

Philips, A.K.; Ahvenainen, M.; Doagu, F.; Järvelä, I.; Sirén, A.; Avela, K.; Somer, M.; Peippo, M.; Kääriäinen, H.; Arvio, M.; Van Esch, H.; Froyen, G.; Haas, S.A.; Hu, H.; Kalscheuer, V.M.

Source

In: Orphanet Journal of Rare Diseases. (Orphanet Journal of Rare Diseases, 11 April 2014, 9(1))

Subject

Language

English

ISSN

17501172

Online Access

EBSCOHost PDF Full Text (ProQuest Central) Full Text (Gale Academic Onefile) Open Access (BioMed Central) Web of Science JCR 저널정보 Scopus Find it@PNU

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