WNT10A mutations also associated with agenesis of the maxillary permanent canines, a separate entity

بواسطة Kantaputra P., Kaewgahya M., Kantaputra W.
منشور في 2014

Tricho-odonto-onycho-dermal dysplasia and WNT10A mutations

بواسطة Kantaputra P., Kaewgahya M., Jotikasthira D., Kantaputra W.
منشور في 2014

Effect of migration patterns on maternal genetic structure: A case of Tai-Kadai migration from China to Thailand

بواسطة Kampuansai J., Kutanan W., Tassi F., Kaewgahya M., Ghirotto S., Kangwanpong D.
منشور في 2017

Enamel-renal-gingival syndrome and FAM20A mutations

بواسطة Kantaputra P.N., Kaewgahya M., Khemaleelakul U., Dejkhamron P., Sutthimethakorn S., Thongboonkerd V., Iamaroon A.
منشور في 2014

Enamel-renal-gingival syndrome and FAM20A mutations

بواسطة Kantaputra P.N., Kaewgahya M., Khemaleelakul U., Dejkhamron P., Sutthimethakorn S., Thongboonkerd V., Iamaroon A.
منشور في 2014

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

بواسطة Kantaputra P., Kapoor S., Verma P., Kaewgahya M., Kawasaki K., Ohazama A., Ketudat Cairns J.
منشور في 2017

TFAP2B mutation and dental anomalies

بواسطة Tanasubsinn N., Sittiwangkul R., Pongprot Y., Kawasaki K., Ohazama A., Sastraruji T., Kaewgahya M., Kantaputra P.
منشور في 2017

Cutis laxa with pulmonary emphysema, conjunctivochalasis, nasolacrimal duct obstruction, abnormal hair, and a novel FBLN5 mutation

بواسطة Kantaputra P.N., Kaewgahya M., Wiwatwongwana A., Wiwatwongwana D., Sittiwangkul R., Iamaroon A., Dejkhamron P.
منشور في 2014

Cutis laxa with pulmonary emphysema, conjunctivochalasis, nasolacrimal duct obstruction, abnormal hair, and a novel FBLN5 mutation

بواسطة Kantaputra P.N., Kaewgahya M., Wiwatwongwana A., Wiwatwongwana D., Sittiwangkul R., Iamaroon A., Dejkhamron P.
منشور في 2014

Cutis laxa with pulmonary emphysema, conjunctivochalasis, nasolacrimal duct obstruction, abnormal hair, and a novel FBLN5 mutation

بواسطة Kantaputra,P.N.I., Kaewgahya,M., Wiwatwongwana,A., Wiwatwongwana,D., Sittiwangkul,R., Iamaroon,A., Dejkhamron,P.
منشور في 2015

Cutis laxa with pulmonary emphysema, conjunctivochalasis, nasolacrimal duct obstruction, abnormal hair, and a novel FBLN5 mutation

بواسطة Kantaputra,P.N.I., Kaewgahya,M., Wiwatwongwana,A., Wiwatwongwana,D., Sittiwangkul,R., Iamaroon,A., Dejkhamron,P.
منشور في 2015

Periodontal disease and FAM20A mutations

بواسطة Kantaputra P., Bongkochwilawan C., Lubinsky M., Pata S., Kaewgahya M., Tong H., Ketudat Cairns J., Guven Y., Chaisrisookumporn N.
منشور في 2017

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

بواسطة Kantaputra P.N., Bongkochwilawan C., Kaewgahya M., Ohazama A., Kayserili H., Erdem A.P., Aktoren O., Guven Y.
منشور في 2014