N. Okamoto

Cohen syndrome with high urinary excretion of hyaluronic acid.

H. Arai, N. Okamoto, Y. Hatsukawa, 1998, American journal of medical genetics.

[Norrie disease].

N. Okamoto, 1998, Ryoikibetsu shokogun shirizu.

Hydrocephalus and Hirschsprung's disease in a patient with a mutation of L1CAM.

Y. Wada, N. Okamoto, N. Okamoto, 1997, Journal of medical genetics.

Brachmann-de Lange syndrome and congenital heart disease.

M. Masuno, Y. Kuroki, I. Kondo, 1998, American journal of medical genetics.

New MCA/MR syndrome with generalized hypotonia, congenital hydronephrosis, and characteristic face.

K. Shimada, F. Matsumoto, K. Satomura, 1997, American journal of medical genetics.