Browsing by Author Warissara Sripathomsawat

Jump to: 0-9 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
or enter first few letters:  
Showing results 2 to 7 of 7 < previous 
Issue DateTitleAuthor(s)
1-Jun-2011Mutation in SAM domain of TP63 is associated with nonsyndromic cleft lip and palate and cleft palatePiranit N. Kantaputra; Sutti Malaivijitnond; Alexandre R. Vieira; Jan Heering; Volker Dötsch; Theerapong Khankasikum; Warissara Sripathomsawat
1-Nov-2010A novel homozygous Arg222Trp missense mutation in WNT7A in two sisters with severe Al-Awadi/Raas-Rothschild/Schinzel phocomelia syndromePiranit N. Kantaputra; Stefan Mundlos; Warissara Sripathomsawat
1-Jan-2011Phenotypic analysis of Arg227 mutations of TP63 with emphasis on dental phenotype and micturition difficulties in EEC syndromeWarissara Sripathomsawat; Pranoot Tanpaiboon; Jan Heering; Volker Dötsch; Raoul C M Hennekam; Piranit Kantaputra
1-Jan-2012Split hand-split foot-ectodermal dysplasia and amelogenesis imperfecta with a TP63 mutationPiranit N. Kantaputra; Oranart Matangkasombut; Warissara Sripathomsawat
2010TP63 mutation in patients with syndromic and non-syndromic hypodontia and cleft lip and palate = การกลายพันธุ์ของยีน TP63 ในผู้ป่วยที่มีภาวะฟันหายแต่ กำเนิดและปากแหว่งและเพดานโหว่ทั้งที่ร่วมและไม่ร่วมกับกลุ่มอาการอื่น / Warissara SripathomsawatWarissara Sripathomsawat
1-May-2011WNT10A and isolated hypodontiaPiranit Kantaputra; Warissara Sripathomsawat