WNT10A and isolated hypodontia

由 Kantaputra P., Sripathomsawat W.
出版 2017

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

由 Kantaputra P.N., Mundlos S., Sripathomsawat W.
出版 2014

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

由 Kantaputra P.N., Matangkasombut O., Sripathomsawat W.
出版 2014

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

由 Tanpaiboon P., Sittiwangkul R., Dejkhamron P., Srikummool M., Sripathomsawat W., Kantaputra P.
出版 2014

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

由 Sripathomsawat W., Tanpaiboon P., Heering J., Dotsch V., Hennekam R.C., Kantaputra P.
出版 2014

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

由 Kantaputra P.N., Malaivijitnond S., Vieira A.R., Heering J., Dotsch V., Khankasikum T., Sripathomsawat W.
出版 2014