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SNP array-based homozygosity mapping reveals MCPH1 deletion in family with autosomal recessive mental retardation and mild microcephaly

Document Type

Journal

Author

Garshasbi, M; Motazacker, MM; Kahrizi, K; Behjati, F; Abedini, SS; Nieh, SE; Firouzabadi, SG; Becker, C; Ruschendorf, F; Nurnberg, P; Tzschach, A; Vazifehmand, R; Erdogan, F; Ullmann, R; Lenzner, S; Kuss, AW; Ropers, HH; Najmabadi, H

Source

HUMAN GENETICS; FEB 2006, 118 6, p708-p715, 8p.

Subject

Language

English

ISSN

03406717

Online Access

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

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