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P N Kantaputra

Showing results (1-10 of 17) with videos related to

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American Journal of Medical Genetics|February 13, 2001
Laurin-Sandrow syndrome with additional associated manifestationsP N Kantaputra
Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology, and Endodontics|September 12, 2001
A newly recognized syndrome of skeletal dysplasia with opalescent and rootless teethP N Kantaputra
Clinical Dysmorphology|May 13, 1999
Juberg-Hayward syndrome: a new case report and clinical delineation of the syndromeP N Kantaputra, S Mongkolchaisup
American Journal of Medical Genetics|June 27, 2000
Are triphalangeal thumb-polysyndactyly syndrome (TPTPS) and tibial hemimelia-polysyndactyly-triphalangeal thumb syndrome (THPTTS) identical? A father with TPTPS and his daughter with THPTTS in a Thai familyP N Kantaputra, P Chalidapong
Clinical Dysmorphology|July 1, 1992
Double dens invaginatus of molarized maxillary central incisors, premolarization of maxillary lateral incisors, multituberculism of the mandibular incisors, canines and first premolar, and sensorineural hearing lossP N Kantaputra, R J Gorlin
American Journal of Medical Genetics|October 21, 1998
Rapp-Hodgkin syndrome with palmoplantar keratoderma, glossy tongue, congenital absence of lingual frenum and of sublingual caruncles: newly recognized findingsP N Kantaputra, C Pruksachatkunakorn, P Vanittanakom
Clinical Dysmorphology|July 12, 2001
Digitotalar dysmorphism with craniofacial and other new associated abnormalitiesP N Kantaputra, P Chalidapong, P Visrutaratna
American Journal of Medical Genetics|December 18, 2001
Mental retardation, obesity, mandibular prognathism with eye and skin anomalies (MOMES syndrome): a newly recognized autosomal recessive syndromeP N Kantaputra, J Kunachaichote, P Patikulsila
American Journal of Medical Genetics|December 11, 1992
Dominant mesomelic dysplasia, ankle, carpal, and tarsal synostosis type: a new autosomal dominant bone disorderP N Kantaputra, R J Gorlin, L O Langer
Journal of Dental Research|May 27, 2003
Heterozygous mutation in the SAM domain of p63 underlies Rapp-Hodgkin ectodermal dysplasiaP N Kantaputra, T Hamada, T Kumchai, et al.
Pageof 2

Showing results (1-10 of 17) with videos related to

Sort By:
Pageof 2
American Journal of Medical Genetics|February 13, 2001
Laurin-Sandrow syndrome with additional associated manifestationsP N Kantaputra
Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology, and Endodontics|September 12, 2001
A newly recognized syndrome of skeletal dysplasia with opalescent and rootless teethP N Kantaputra
Clinical Dysmorphology|May 13, 1999
Juberg-Hayward syndrome: a new case report and clinical delineation of the syndromeP N Kantaputra, S Mongkolchaisup
American Journal of Medical Genetics|June 27, 2000
Are triphalangeal thumb-polysyndactyly syndrome (TPTPS) and tibial hemimelia-polysyndactyly-triphalangeal thumb syndrome (THPTTS) identical? A father with TPTPS and his daughter with THPTTS in a Thai familyP N Kantaputra, P Chalidapong
Clinical Dysmorphology|July 1, 1992
Double dens invaginatus of molarized maxillary central incisors, premolarization of maxillary lateral incisors, multituberculism of the mandibular incisors, canines and first premolar, and sensorineural hearing lossP N Kantaputra, R J Gorlin
American Journal of Medical Genetics|October 21, 1998
Rapp-Hodgkin syndrome with palmoplantar keratoderma, glossy tongue, congenital absence of lingual frenum and of sublingual caruncles: newly recognized findingsP N Kantaputra, C Pruksachatkunakorn, P Vanittanakom
Clinical Dysmorphology|July 12, 2001
Digitotalar dysmorphism with craniofacial and other new associated abnormalitiesP N Kantaputra, P Chalidapong, P Visrutaratna
American Journal of Medical Genetics|December 18, 2001
Mental retardation, obesity, mandibular prognathism with eye and skin anomalies (MOMES syndrome): a newly recognized autosomal recessive syndromeP N Kantaputra, J Kunachaichote, P Patikulsila
American Journal of Medical Genetics|December 11, 1992
Dominant mesomelic dysplasia, ankle, carpal, and tarsal synostosis type: a new autosomal dominant bone disorderP N Kantaputra, R J Gorlin, L O Langer
Journal of Dental Research|May 27, 2003
Heterozygous mutation in the SAM domain of p63 underlies Rapp-Hodgkin ectodermal dysplasiaP N Kantaputra, T Hamada, T Kumchai, et al.
Pageof 2