WNT10A and isolated hypodontia

by Piranit Kantaputra, Warissara Sripathomsawat
Published 2018

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

by Piranit N. Kantaputra, Stefan Mundlos, Warissara Sripathomsawat
Published 2018

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

by Piranit N. Kantaputra, Oranart Matangkasombut, Warissara Sripathomsawat
Published 2018

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

by Pranoot Tanpaiboon, Rekwan Sittiwangkul, Prapai Dejkhamron, Metawee Srikummool, Warissara Sripathomsawat, Piranit Kantaputra
Published 2018

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

by Pranoot Tanpaiboon, Rekwan Sittiwangkul, Prapai Dejkhamron, Metawee Srikummool, Warissara Sripathomsawat, Piranit Kantaputra
Published 2018

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

by Warissara Sripathomsawat, Pranoot Tanpaiboon, Jan Heering, Volker Dötsch, Raoul C M Hennekam, Piranit Kantaputra
Published 2018

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

by Piranit N. Kantaputra, Sutti Malaivijitnond, Alexandre R. Vieira, Jan Heering, Volker Dötsch, Theerapong Khankasikum, Warissara Sripathomsawat
Published 2018