| ปี พ.ศ. 2557 |
| 1 |
BCOR mutations and unstoppable root growth: A commentary on oculofaciocardiodental syndrome: Novel BCOR mutations and expression in dental cells |
| 2 |
Clinical manifestations of 17 patients affected with mucopolysaccharidosis type VI and eight novel ARSB mutations |
| 3 |
Twins with hereditary sensory and autonomic neuropathy type IV with preserved periodontal sensation |
| 4 |
Enamel-renal-gingival syndrome and FAM20A mutations |
| 5 |
Enamel-renal-gingival syndrome and FAM20A mutations |
| 6 |
Oral manifestations of 17 patients affected with mucopolysaccharidosis type VI |
| 7 |
Split hand-split foot-ectodermal dysplasia and amelogenesis imperfecta with a TP63 mutation |
| 8 |
Enamel-Renal-Gingival syndrome, hypodontia, and a novel FAM20A mutation |
| 9 |
Cutis laxa with pulmonary emphysema, conjunctivochalasis, nasolacrimal duct obstruction, abnormal hair, and a novel FBLN5 mutation |
| 10 |
Cutis laxa with pulmonary emphysema, conjunctivochalasis, nasolacrimal duct obstruction, abnormal hair, and a novel FBLN5 mutation |
| ปี พ.ศ. 2556 |
| 11 |
A novel mutation in CDKN1C in sibs with Beckwith-Wiedemann syndrome and cleft palate, sensorineural hearing loss, and supernumerary flexion creases |
| 12 |
A novel mutation in CDKN1C in sibs with Beckwith-Wiedemann syndrome and cleft palate, sensorineural hearing loss, and supernumerary flexion creases |
| ปี พ.ศ. 2555 |
| 13 |
Dyschromatosis symmetrica hereditaria with long hair on the forearms, hypo/hyperpigmented hair, and dental anomalies: Report of a novel ADAR1 mutation |
| 14 |
Multiple supernumerary molars, anterior openbite, and large ear lobules in mucopolysaccharidosis type VI patient |
| 15 |
Severe plexiform facial neurofibromatosis, type 1 with underdeveloped eyes and a novel NF1 mutation |
| ปี พ.ศ. 2554 |
| 16 |
Mutation in SAM domain of TP63 is associated with nonsyndromic cleft lip and palate and cleft palate |
| 17 |
Cleft lip with cleft palate, ankyloglossia, and hypodontia are associated with TBX22 mutations |
| ปี พ.ศ. 2553 |
| 18 |
A novel homozygous Arg222Trp missense mutation in WNT7A in two sisters with severe Al-Awadi/Raas-Rothschild/Schinzel phocomelia syndrome |
| 19 |
Mesomelic dysplasia Kantaputra type is associated with duplications of the HOXD locus on chromosome 2q |
| ปี พ.ศ. 2550 |
| 20 |
Children's attitudes toward behavior management techniques used by dentists |
| 21 |
Children's attitudes toward behavior management techniques used by dentists |
| ปี พ.ศ. 2549 |
| 22 |
A newly recognized polyosteolysis/hyperostosis syndrome |
| ปี พ.ศ. 2548 |
| 23 |
A newly recognized syndrome involving limbs, pelvis, and genital organs or a variant of Al-Awadi/Raas-Rothschild syndrome? |
| 24 |
Re: Microcephalic osteodysplastic primordial dwarfism with severe microdontia and skin anomalies [Kantaputra et al. 2004. Am J Med Genet 130A:181-190] [4] (multiple letters) |
| 25 |
A newly recognized syndrome involving limbs, pelvis, and genital organs or a variant of Al-Awadi/Raas-Rothschild syndrome? |
| ปี พ.ศ. 2547 |
| 26 |
Microcephalic osteodysplastic primordial dwarfism with severe microdontia and skin anomalies: Confirmation of a new syndrome |
| 27 |
Thirteen-year-follow up report on mesomelic dysplasia, Kantaputra type (MDK), and comments on the paper of the second reported family of MDK by Shears et al. |
| 28 |
Microcephalic osteodysplastic primordial dwarfism with severe microdontia and skin anomalies: Confirmation of a new syndrome |
| 29 |
Thirteen-year-follow up report on mesomelic dysplasia, Kantaputra type (MDK), and comments on the paper of the second reported family of MDK by Shears et al |
| ปี พ.ศ. 2546 |
| 30 |
Heterozygous mutation in the SAM domain of p63 underlies Rapp-Hodgkin ectodermal dysplasia |
| 31 |
A new syndrome of symphalangism, multiple frenula, postaxial polydactyly, dysplastic ears, dental anomalies, and exclusion of NOG and GDF5 |
| 32 |
A new syndrome of symphalangism, multiple frenula, postaxial polydactyly, dysplastic ears, dental anomalies, and exclusion of NOG and GDF5 |
| ปี พ.ศ. 2545 |
| 33 |
Van der Woude syndrome with sensorineural hearing loss, large craniofacial sinuses, dental pulp stones, and minor limb anomalies: Report of a four-generation Thai family |
| 34 |
A Thai mother and son with distal symphalangism, hypoplastic carpal bones, microdontia, dental pulp stones, and narrowing of the zygomatic arch: A new distal symphalangism syndrome? |
| 35 |
Van der Woude syndrome with sensorineural hearing loss, large craniofacial sinuses, dental pulp stones, and minor limb anomalies: Report of a four-generation Thai family |
| 36 |
A novel gene is disrupted at a 14q13 breakpoint of t(2;14) in a patient with mirror-image polydactyly of hands and feet |
| 37 |
A dominantly inherited malformation syndrome with short stature, upper limb anomaly, minor craniofacial anomalies, and absence of TBX5 mutations: Report of a Thai family |
| 38 |
Apparently new osteodysplastic and primordial short stature with severe microdontia, opalescent teeth, and rootless molars in two siblings |
| ปี พ.ศ. 2544 |
| 39 |
Digitotalar dysmorphism with craniofacial and other new associated abnormalities |
| 40 |
Laurin-Sandrow syndrome with additional associated manifestations |
| 41 |
Mental retardation, obesity, mandibular prognathism with eye and skin anomalies (MOMES Syndrome): A newly recognized autosomal recessive syndrome |
| 42 |
Cryptophthalmos, dental and oral abnormalities, and brachymesophalangy of second toes: New syndrome or Fraser syndrome? |
| 43 |
A newly recognized syndrome of skeletal dysplasia with opalescent and rootless teeth |
| 44 |
Mental retardation, obesity, mandibular prognathism with eye and skin anomalies (MOMES Syndrome): A newly recognized autosomal recessive syndrome |
| 45 |
Dentinogenesis imperfecta-associated syndromes |
| 46 |
Cryptophthalmos, dental and oral abnormalities, and brachymesophalangy of second toes: New syndrome or Fraser syndrome? |
| 47 |
Digitotalar dysmorphism with craniofacial and other new associated abnormalities |
| ปี พ.ศ. 2543 |
| 48 |
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 |
| ปี พ.ศ. 2542 |
| 49 |
Juberg-Hayward syndrome: a new case report and clinical delineation of the syndrome |
| 50 |
Robinow (fetal face) syndrome: report of a boy with dominant type and an infant with recessive type |
| ปี พ.ศ. 2541 |
| 51 |
Rapp-Hodgkin syndrome with palmoplantar keratoderma, glossy tongue, congenital absence of lingual frenum and of sublingual caruncles: newly recognized findings |
