M. Touyama

Trends in the prevalence of cerebral palsy in children born between 1988 and 2007 in Okinawa, Japan

Yasuki Kobayashi, S. Toyokawa, M. Touyama, 2016, Brain and Development.

Fifty microdeletions among 112 cases of Sotos syndrome: Low copy repeats possibly mediate the common deletion

Jan-Fang Cheng, Naomichi Matsumoto, Kenji Kurosawa, 2003, Human mutation.

Preferential paternal origin of microdeletions caused by prezygotic chromosome or chromatid rearrangements in Sotos syndrome.

Y. Fukushima, N. Niikawa, T. Shiihara, 2003, American journal of human genetics.

Missense mutations in the DNA-binding/dimerization domain of NFIX cause Sotos-like features

N. Matsumoto, K. Ogata, Y. Makita, 2012, Journal of Human Genetics.

[Cerebral palsy in twins in Okinawa].

M. Touyama, J. Touyama, Y. Ochiai, 2000, No to hattatsu = Brain and development.

Phenotypic consequences of genetic variation at hemizygous alleles: Sotos syndrome is a contiguous gene syndrome incorporating coagulation factor twelve (FXII) deficiency

J. Lupski, T. Shiihara, Y. Makita, 2005, Genetics in Medicine.

Long‐term survival of children with cerebral palsy in Okinawa, Japan

Yasuki Kobayashi, S. Toyokawa, M. Touyama, 2013, Developmental medicine and child neurology.