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Piranit Kantaputra

Showing results (1-10 of 37) with videos related to

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American Journal of Medical Genetics. Part A|September 11, 2003
Thyroid dysfunction in a patient with aglossiaPiranit Kantaputra, Pranoot Tanpaiboon
American Journal of Medical Genetics. Part A|April 13, 2011
WNT10A and isolated hypodontiaPiranit Kantaputra, Warissara Sripathomsawat
The Journal of Dermatology|February 22, 2022
WNT10A variant and severe scoliosis?Piranit Kantaputra, Bjorn Olsen, John A McGrath
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|March 8, 2011
TBX22 mutation associated with cleft lip/palate, hypodontia, and limb anomalyArunee Kaewkhampa, Dhirawat Jotikasthira, Sutti Malaivijitnond, et al.
American Journal of Medical Genetics. Part A|February 27, 2010
c. 595-596 insC of FOXC2 underlies lymphedema, distichiasis, ptosis, ankyloglossia, and Robin sequence in a Thai patientPranoot Tanpaiboon, Piranit Kantaputra, Karn Wejathikul, et al.
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|January 5, 2011
Phenotypic analysis of Arg227 mutations of TP63 with emphasis on dental phenotype and micturition difficulties in EEC syndromeWarissara Sripathomsawat, Pranoot Tanpaiboon, Jan Heering, et al.
The Journal of Dermatology|March 29, 2020
Clouston syndrome with pili canaliculi, pili torti, overgrown hyponychium, onycholysis, taurodontism and absence of palmoplantar keratodermaPiranit Kantaputra, Worrachet Intachai, Katsushige Kawasaki, et al.
American Journal of Medical Genetics. Part A|May 14, 2011
The smallest teeth in the world are caused by mutations in the PCNT genePiranit Kantaputra, Pranoot Tanpaiboon, Thantrira Porntaveetus, et al.
Briefings in Functional Genomics|October 28, 2022
Core promoter in TNBC is highly mutated with rich ethnic signatureTeng Huang, Jiaheng Li, Heng Zhao, et al.
Pageof 4

Showing results (1-10 of 37) with videos related to

Sort By:
Pageof 4
American Journal of Medical Genetics. Part A|September 11, 2003
Thyroid dysfunction in a patient with aglossiaPiranit Kantaputra, Pranoot Tanpaiboon
American Journal of Medical Genetics. Part A|April 13, 2011
WNT10A and isolated hypodontiaPiranit Kantaputra, Warissara Sripathomsawat
The Journal of Dermatology|February 22, 2022
WNT10A variant and severe scoliosis?Piranit Kantaputra, Bjorn Olsen, John A McGrath
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|March 8, 2011
TBX22 mutation associated with cleft lip/palate, hypodontia, and limb anomalyArunee Kaewkhampa, Dhirawat Jotikasthira, Sutti Malaivijitnond, et al.
American Journal of Medical Genetics. Part A|February 27, 2010
c. 595-596 insC of FOXC2 underlies lymphedema, distichiasis, ptosis, ankyloglossia, and Robin sequence in a Thai patientPranoot Tanpaiboon, Piranit Kantaputra, Karn Wejathikul, et al.
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|January 5, 2011
Phenotypic analysis of Arg227 mutations of TP63 with emphasis on dental phenotype and micturition difficulties in EEC syndromeWarissara Sripathomsawat, Pranoot Tanpaiboon, Jan Heering, et al.
The Journal of Dermatology|March 29, 2020
Clouston syndrome with pili canaliculi, pili torti, overgrown hyponychium, onycholysis, taurodontism and absence of palmoplantar keratodermaPiranit Kantaputra, Worrachet Intachai, Katsushige Kawasaki, et al.
American Journal of Medical Genetics. Part A|May 14, 2011
The smallest teeth in the world are caused by mutations in the PCNT genePiranit Kantaputra, Pranoot Tanpaiboon, Thantrira Porntaveetus, et al.
Briefings in Functional Genomics|October 28, 2022
Core promoter in TNBC is highly mutated with rich ethnic signatureTeng Huang, Jiaheng Li, Heng Zhao, et al.
Pageof 4