Warissara Sripathomsawat

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

V. Dötsch, P. Kantaputra, A. R. Vieira, 2011, American journal of medical genetics. Part A.

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

R. Hennekam, V. Dötsch, P. Tanpaiboon, 2011, American journal of medical genetics. Part A.

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

S. Mundlos, P. Kantaputra, Warissara Sripathomsawat, 2010, American journal of medical genetics. Part A.

WNT10A and isolated hypodontia

P. Kantaputra, Warissara Sripathomsawat, 2011, American journal of medical genetics. Part A.

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

O. Matangkasombut, P. Kantaputra, Warissara Sripathomsawat, 2012, American journal of medical genetics. Part A.

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

P. Tanpaiboon, R. Sittiwangkul, P. Kantaputra, 2009, American journal of medical genetics. Part A.