WNT10A and isolated hypodontia

بواسطة Kantaputra P., Sripathomsawat W.
منشور في 2017

A novel homozygous Arg222Trp missense mutation in WNT7A in two sisters with severe Al-Awadi/Raas-Rothschild/Schinzel phocomelia syndrome

بواسطة Kantaputra P.N., Mundlos S., Sripathomsawat W.
منشور في 2014

Split hand-split foot-ectodermal dysplasia and amelogenesis imperfecta with a TP63 mutation

بواسطة Kantaputra P.N., Matangkasombut O., Sripathomsawat W.
منشور في 2014

Expanding the phenotypic spectrum of acro-cardio-facial syndrome (ACFS): Exclusion of P63 mutation

بواسطة Tanpaiboon P., Sittiwangkul R., Dejkhamron P., Srikummool M., Sripathomsawat W., Kantaputra P.
منشور في 2014

Phenotypic analysis of Arg227 mutations of TP63 with emphasis on dental phenotype and micturition difficulties in EEC syndrome

بواسطة Sripathomsawat W., Tanpaiboon P., Heering J., Dotsch V., Hennekam R.C., Kantaputra P.
منشور في 2014

Mutation in SAM domain of TP63 is associated with nonsyndromic cleft lip and palate and cleft palate

بواسطة Kantaputra P.N., Malaivijitnond S., Vieira A.R., Heering J., Dotsch V., Khankasikum T., Sripathomsawat W.
منشور في 2014