Intragenic microdeletion of RUNX2 is a novel mechanism for cleidocranial dysplasia

Please use this identifier to cite or link to this item: http://ir.sinica.edu.tw/handle/201000000A/22657

Title:	Intragenic microdeletion of RUNX2 is a novel mechanism for cleidocranial dysplasia
Authors:	Lee, M. T. Tsai, A. C. Chou, C. H. Sun, F. M. Huang, L. C. Yen, P. Lin, C. C. Liu, C. Y. Wu, J. Y. Chen, Y. T. Tsai, F. J.
Issue Date:	2008
Relation:	Genomic Med 2(1-2), 45-49
URI:	http://ir.sinica.edu.tw/handle/201000000A/22657
ISSN:	http://gateway.isiknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=Drexel&SrcApp=hagerty_opac&KeyRecord=1871-7934&DestApp=JCR&RQ=IF_CAT_BOXPLOT
URL:	http://www.ncbi.nlm.nih.gov/pubmed/18696259
Appears in Collections:	生物醫學科學研究所

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