Koji Muroya

CAG repeat length analysis and mutation screening of the androgen receptor gene in Japanese men with idiopathic azoospermia.

T. Ogata, T. Nakada, I. Sasagawa, 2001, Journal of andrology.

Mutation screening and CAG repeat length analysis of the androgen receptor gene in Klinefelter's syndrome patients with and without spermatogenesis.

T. Ogata, T. Nakada, I. Sasagawa, 2001, Human reproduction.

Skeletal features and growth patterns in 14 patients with haploinsufficiency of SHOX: implications for the development of Turner syndrome.

T. Ogata, H. Ohashi, G. Nishimura, 1999, The Journal of clinical endocrinology and metabolism.

Random X-inactivation in a girl with duplication Xp11.21-p21.3: report of a patient and review of the literature.

Y. Fukushima, T. Ogata, K. Kosaki, 1999, American journal of medical genetics.

Identification of mutations in the hepatocyte nuclear factor-1alpha gene in Japanese subjects with early-onset NIDDM and functional analysis of the mutant proteins.

T. Takumi, T. Ogata, N. Iwatani, 1999, Diabetes.