Phenotypic spectrum of CHARGE syndrome with CHD7 mutationsMichihiko Aramaki, Kenjiro Kosaki, Nobuko Moriyama et al.|The Journal of Pediatrics|2006Cited by 168
Embryonic expression profile of chicken <i>CHD7</i>, the ortholog of the causative gene for CHARGE syndromeMichihiko Aramaki, Kenjiro Kosaki, Toru Udaka et al.|Birth Defects Research Part A Clinical and Molecular Teratology|2006Cited by 42
Large fontanelles are a shared feature of haploinsufficiency of <i>RUNX2</i> and its co‐activator <i>CBFB</i>Tomohide Goto, Kenjiro Kosaki, Michihiko Aramaki et al.|Congenital Anomalies|2004Cited by 27
Iridic and retinal coloboma associated with prenatal methimazole exposureMichihiko Aramaki, Kenjiro Kosaki, Isamu Hokuto et al.|American Journal of Medical Genetics Part A|2005Cited by 24