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Haploinsufficiency of novel FOXG1B variants in a patient with severe mental retardation, brain malformations and microcephaly

Document Type

Journal

Author

Shoichet, SA; Kunde, SA; Viertel, P; Schell-Apacik, C; von Voss, H; Tommerup, N; Ropers, HH; Kalscheuer, VM

Source

HUMAN GENETICS; OCT 2005, 117 6, p536-p544, 9p.

Subject

Language

English

ISSN

03406717

Online Access

Full Text (ProQuest Central) Full Text (Springer-Archive) Web of Science JCR 저널정보 Scopus Find it@PNU

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