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Warissara Sripathomsawat

Showing results (1-10 of 5) with videos related to

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American Journal of Medical Genetics. Part A|April 13, 2011
WNT10A and isolated hypodontiaPiranit Kantaputra, Warissara Sripathomsawat
American Journal of Medical Genetics. Part A|November 9, 2011
Split hand-split foot-ectodermal dysplasia and amelogenesis imperfecta with a TP63 mutationPiranit N Kantaputra, Oranart Matangkasombut, Warissara Sripathomsawat
American Journal of Medical Genetics. Part A|October 16, 2010
A 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
American Journal of Medical Genetics. Part A|July 17, 2009
Expanding the phenotypic spectrum of acro-cardio-facial syndrome (ACFS): Exclusion of P63 mutationPranoot Tanpaiboon, Rekwan Sittiwangkul, Prapai Dejkhamron, et al.
American Journal of Medical Genetics. Part A|May 14, 2011
Mutation in SAM domain of TP63 is associated with nonsyndromic cleft lip and palate and cleft palatePiranit N Kantaputra, Sutti Malaivijitnond, Alexandre R Vieira, et al.
Pageof 1

Showing results (1-10 of 5) with videos related to

Sort By:
Pageof 1
American Journal of Medical Genetics. Part A|April 13, 2011
WNT10A and isolated hypodontiaPiranit Kantaputra, Warissara Sripathomsawat
American Journal of Medical Genetics. Part A|November 9, 2011
Split hand-split foot-ectodermal dysplasia and amelogenesis imperfecta with a TP63 mutationPiranit N Kantaputra, Oranart Matangkasombut, Warissara Sripathomsawat
American Journal of Medical Genetics. Part A|October 16, 2010
A 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
American Journal of Medical Genetics. Part A|July 17, 2009
Expanding the phenotypic spectrum of acro-cardio-facial syndrome (ACFS): Exclusion of P63 mutationPranoot Tanpaiboon, Rekwan Sittiwangkul, Prapai Dejkhamron, et al.
American Journal of Medical Genetics. Part A|May 14, 2011
Mutation in SAM domain of TP63 is associated with nonsyndromic cleft lip and palate and cleft palatePiranit N Kantaputra, Sutti Malaivijitnond, Alexandre R Vieira, et al.
Pageof 1