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Nature Genetics|February 2, 2000
Gene-target recognition among members of the myc superfamily and implications for oncogenesisR C O'Hagan, N Schreiber-Agus, K Chen, et al.Nature Genetics|February 2, 2000
Aberrant CpG-island methylation has non-random and tumour-type-specific patternsJ F Costello, M C Frühwald, D J Smiraglia, et al.Nature Genetics|February 2, 2000
A new gene involved in X-linked mental retardation identified by analysis of an X;2 balanced translocationR Zemni, T Bienvenu, M C Vinet, et al.Nature Genetics|February 2, 2000
Heritable and inducible genetic interference by double-stranded RNA encoded by transgenesN Tavernarakis, S L Wang, M Dorovkov, et al.Nature Genetics|February 2, 2000
Transport of lipids from golgi to plasma membrane is defective in tangier disease patients and Abc1-deficient miceE Orsó, C Broccardo, W E Kaminski, et al.Nature Genetics|March 4, 2000
Dominant mutations in ROR2, encoding an orphan receptor tyrosine kinase, cause brachydactyly type BM Oldridge, A M Fortuna, M Maringa, et al.Nature Genetics|March 4, 2000
Mutations in a new gene in Ellis-van Creveld syndrome and Weyers acrodental dysostosisV L Ruiz-Perez, S E Ide, T M Strom, et al.Nature Genetics|March 4, 2000
Mice mutant for Egfr and Shp2 have defective cardiac semilunar valvulogenesisB Chen, R T Bronson, L D Klaman, et al.Nature Genetics|March 4, 2000
Mice deficient in Abl are osteoporotic and have defects in osteoblast maturationB Li, S Boast, K de los Santos, et al.Nature Genetics|March 4, 2000
Mekk3 is essential for early embryonic cardiovascular developmentJ Yang, M Boerm, M McCarty, et al.Pageof 745