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Browsing by Author Warissara Sripathomsawat

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Showing results 1 to 7 of 7

Issue Date	Title	Author(s)
1-Aug-2009	Expanding the phenotypic spectrum of acro-cardio-facial syndrome (ACFS): Exclusion of P63 mutation	Pranoot Tanpaiboon; Rekwan Sittiwangkul; Prapai Dejkhamron; Metawee Srikummool; Warissara Sripathomsawat; Piranit Kantaputra
1-Jun-2011	Mutation in SAM domain of TP63 is associated with nonsyndromic cleft lip and palate and cleft palate	Piranit N. Kantaputra; Sutti Malaivijitnond; Alexandre R. Vieira; Jan Heering; Volker Dötsch; Theerapong Khankasikum; Warissara Sripathomsawat
1-Nov-2010	A novel homozygous Arg222Trp missense mutation in WNT7A in two sisters with severe Al-Awadi/Raas-Rothschild/Schinzel phocomelia syndrome	Piranit N. Kantaputra; Stefan Mundlos; Warissara Sripathomsawat
1-Jan-2011	Phenotypic analysis of Arg227 mutations of TP63 with emphasis on dental phenotype and micturition difficulties in EEC syndrome	Warissara Sripathomsawat; Pranoot Tanpaiboon; Jan Heering; Volker Dötsch; Raoul C M Hennekam; Piranit Kantaputra
1-Jan-2012	Split hand-split foot-ectodermal dysplasia and amelogenesis imperfecta with a TP63 mutation	Piranit N. Kantaputra; Oranart Matangkasombut; Warissara Sripathomsawat
2010	TP63 mutation in patients with syndromic and non-syndromic hypodontia and cleft lip and palate = การกลายพันธุ์ของยีน TP63 ในผู้ป่วยที่มีภาวะฟันหายแต่ กำเนิดและปากแหว่งและเพดานโหว่ทั้งที่ร่วมและไม่ร่วมกับกลุ่มอาการอื่น / Warissara Sripathomsawat	Warissara Sripathomsawat
1-May-2011	WNT10A and isolated hypodontia	Piranit Kantaputra; Warissara Sripathomsawat

Showing results 1 to 7 of 7