In the October 2002 issue of the Journal, in the article “Functional Analysis of RUNX2 Mutations in Japanese Patients with Cleidocranial Dysplasia Demonstrates Novel Genotype-Phenotype Correlations,” by Yoshida et al. (71:724–738), the reference cited as “Yoshida et al., in press” should be supplemented with two related references: Kundu et al. (2002) and Miller et al. (2002). (“Yoshida et al., in press” was cited at two places in the text, the last line in the first paragraph of p. 725 and the last line in the second paragraph of p. 735.) The updated full data of these three references are as follows:
References
- Kundu M, Javed A, Jeon JP, Horner A, Shum L, Eckhaus M, Muenke M, Lian JB, Yang Y, Nuckolls GH, Stein GS, Liu PP (2002) Cbfβ interacts with Runx2 and has a critical role in bone development. Nat Genet 32:639–644 [DOI] [PubMed] [Google Scholar]
- Miller J, Horner A, Stacy T, Lowrey C, Lian JB, Stein GS, Nuckolls GH, Speck NA (2002) The core-binding factor β subunit is required for bone formation and hematopoietic maturation. Nat Genet 32:645–649 [DOI] [PubMed] [Google Scholar]
- Yoshida CA, Furuichi T, Fujita T, Fukuyama R, Kanatani N, Kobayashi S, Satake M, Takada K, Komori T (2002) Core-binding factor β interacts with Runx2 and is required for skeletal development. Nat Genet 32:633–638 [DOI] [PubMed] [Google Scholar]