K. Maeda

Association of the MSX2 gene polymorphisms with ankylosing spondylitis in Japanese

S. Tsai, K. Ikari, A. Takahashi, 2008, Journal of Human Genetics.

A compound heterozygote harboring novel and recurrent DTDST mutations with intermediate phenotype between atelosteogenesis type II and diastrophic dysplasia

Y. Miyamoto, S. Ikegawa, G. Nishimura, 2006, American journal of medical genetics. Part A.

A large-scale genetic association study of ossification of the posterior longitudinal ligament of the spine

H. Baba, Kozo Nakamura, M. Matsumoto, 2006, Human Genetics.

Novel COL9A3 mutation in a family with multiple epiphyseal dysplasia

R. Kosaki, H. Ohashi, S. Ikegawa, 2005, American journal of medical genetics. Part A.

Novel and recurrent mutations clustered in the von Willebrand factor A domain of MATN3 in multiple epiphyseal dysplasia

R. Kosaki, H. Ohashi, S. Ikegawa, 2004, Human mutation.

MATN and LAPTM are parts of larger transcription units produced by intergenic splicing: intergenic splicing may be a common phenomenon.

Y. Miyamoto, S. Ikegawa, A. Mabuchi, 2006, DNA research : an international journal for rapid publication of reports on genes and genomes.

Mutation in the von Willebrand factor‐A domain is not a prerequisite for the MATN3 mutation in multiple epiphyseal dysplasia

S. Ikegawa, A. Mabuchi, E. Nakashima, 2005, American journal of medical genetics. Part A.

Comprehensive screening of multiple epiphyseal dysplasia mutations in Japanese population

R. Kosaki, H. Ohashi, S. Ikegawa, 2006, American journal of medical genetics. Part A.