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American Journal of Medical Genetics
|
February 13, 2001
Laurin-Sandrow syndrome with additional associated manifestations
P 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 teeth
P N Kantaputra
Clinical Dysmorphology
|
May 13, 1999
Juberg-Hayward syndrome: a new case report and clinical delineation of the syndrome
P 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 family
P 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 loss
P 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 findings
P N Kantaputra, C Pruksachatkunakorn, P Vanittanakom
Clinical Dysmorphology
|
July 12, 2001
Digitotalar dysmorphism with craniofacial and other new associated abnormalities
P 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 syndrome
P 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 disorder
P 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 dysplasia
P N Kantaputra, T Hamada, T Kumchai, et al.
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of 2
Search research articles
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Showing results (1-10 of 17) with videos related to
Sort By:
Page
of 2
American Journal of Medical Genetics
|
February 13, 2001
Laurin-Sandrow syndrome with additional associated manifestations
P 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 teeth
P N Kantaputra
Clinical Dysmorphology
|
May 13, 1999
Juberg-Hayward syndrome: a new case report and clinical delineation of the syndrome
P 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 family
P 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 loss
P 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 findings
P N Kantaputra, C Pruksachatkunakorn, P Vanittanakom
Clinical Dysmorphology
|
July 12, 2001
Digitotalar dysmorphism with craniofacial and other new associated abnormalities
P 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 syndrome
P 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 disorder
P 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 dysplasia
P N Kantaputra, T Hamada, T Kumchai, et al.
Page
of 2