Dyschromatosis symmetrica hereditaria with long hair on the forearms, hypo/hyperpigmented hair, and dental anomalies: Report of a novel ADAR1 mutation

by Kantaputra P.N., Chinadet W., Ohazama A., Kono M.
Published 2014

Al-Awadi-Raas-Rothschild syndrome with dental anomalies and a novel WNT7A mutation

by Kantaputra P., Kapoor S., Verma P., Kaewgahya M., Kawasaki K., Ohazama A., Ketudat Cairns J.
Published 2017

Long-term survival in infantile malignant autosomal recessive osteopetrosis secondary to homozygous p.Arg526Gln mutation in CLCN7

by Kantaputra,P.N.I., Thawanaphong,S., Issarangporn,W., Klangsinsirikul,P., Ohazama,A., Sharpe,P.T., Supanchart,C.
Published 2015

TFAP2B mutation and dental anomalies

by Tanasubsinn N., Sittiwangkul R., Pongprot Y., Kawasaki K., Ohazama A., Sastraruji T., Kaewgahya M., Kantaputra P.
Published 2017

The smallest teeth in the world are caused by mutations in the PCNT gene

by Kantaputra P., Tanpaiboon P., Porntaveetus T., Ohazama A., Sharpe P., Rauch A., Hussadaloy A., Thiel C.T.
Published 2014

Enamel-Renal-Gingival syndrome, hypodontia, and a novel FAM20A mutation

by Kantaputra P.N., Bongkochwilawan C., Kaewgahya M., Ohazama A., Kayserili H., Erdem A.P., Aktoren O., Guven Y.
Published 2014