| [1] |
Sato I, Ishikawa H, Shimada K, Ezure H, Sato T. Morphology and analysis of the development of the human temporomandibular joint and masticatory muscle. Acta Anat (Basel). 1994;149(1):55-62.
|
| [2] |
Steiner CC.Cephalometrics for you and me[J]. Am J Orthod. 1953;39:729–755.
|
| [3] |
Wang Z, Moult J. SNPs, protein structure, and disease[J]. Human Mutat.2001;17:263-70.
|
| [4] |
Ting TY, Wong RWK, Rabie ABM. Analysis of genetic polymorphisms in skeletal Class 1 crowding[J].American Journal of Orthodontics and Dentofacial Orthopedics.2011,140(1):e9-e15.
|
| [5] |
Ardani I, Sanjaya ML, Sjamsudin J. Cephalometric characteristic of skeletal class II malocclusion in Javanese population at Universitas Airlangga Dental Hospital[J]. Contemp Clin Dent. 2018,9(2):S342.
|
| [6] |
Ardani IGAW,Aulanni’am,Diyatri I.Single nucleotide polymorphisms (SNPs) of COL1A1 and COL11A1 in class ii skeletal malocclusion of ethnic Javanese patient[J].Clinical, Cosmetic and Investigational Dentistry,2020,12:173-179.
|
| [7] |
Balkhande PB,LakkakulaBVKS,Chitharanjan AB.Relationship between matrilin-1 gene polymorphisms and mandibular retrognathism[J].American Journal of Orthodontics and Dentofacial Orthopedics,2018,153(2):255-261.
|
| [8] |
Gupta P,Chaturvedi TP,Sharma V.Expressional analysis of MSX1 (Human) revealed its role in sagittal jaw relationship[J].Journal of Clinical and Diagnostic Research,2017,11(8):ZC71-ZC77.
|
| [9] |
Levy SC,Azeredo L,Antunes A,et al.Determination of TNF-α Gene Polymorphisms on Skeletal Pattern in Class II Malocclusion[J].Brazilian Dental Journal (2019) 30(2): 152-156.
|
| [10] |
Jiang Q, Mei L, Zou Y,et al.Genetic Polymorphisms in FGFR2 Underlie Skeletal Malocclusion[J].J Dent Res, 2019 ,98(12):1340-1347.
|
| [11] |
Crozet F, elAmraoui A, Blanchard S, et al. Cloning of the genes encoding twomurine and human cochlear un- conventional type I myosins[J]. Genomics,1997,40:332-41.
|
| [12] |
Arun RM,Lakkakula BVKS,Chitharanjan AB.Role of myosin 1H gene polymorphisms in mandibular retrognathism[J].American Journal of Orthodontics and Dentofacial Orthopedics,2016,149(5):699-704.
|
| [13] |
Sciote JJ,Raoul G,Ferri J.Masseter function and skeletal malocclusion[J].Revue de Stomatologie, de Chirurgie Maxillo-faciale et de Chirurgie Orale,2013,114(2):79-85.
|
| [14] |
Zebrick B,Teeramongkolgul T,Nicot R,et al.ACTN3 R577X genotypes associate with Class II and deepbite malocclusions[J].American Journal of Orthodontics and Dentofacial Orthopedics,2014,146(5),603-611.
|
| [15] |
Lutz J,Nicot R, Schlund M,et al.Dental and Maxillofacial Features of Noonan Syndrome: Case Series of Ten Patients[J].J Craniomaxillofac Surg,2020 Mar;48(3):242-250.
|
| [16] |
Cardiel R, Sergio A.Correction of a severe Class II malocclusion in a patient with Noonan syndrome[J].American Journal of Orthodontics and Dentofacial Orthopedics,2016,150(3):511-520.
|
| [17] |
Cruz RM, Krieger H, Ferreira R,et al. Major gene and multifactorial inheritance of mandibular prognathism[J]. American Journal of Medical Genetics. 2008, 146A(1), 71–77.
|
| [18] |
Kajii TS,Oka A,Saito F,et al.Whole-exome sequencing in a Japanese pedigree implicates a rare non-synonymous single-nucleotide variant in BEST3 as a candidate for mandibular prognathism[J].Bone,2019,122(September 2018):193-198.
|
| [19] |
Kantaputra PN,Pruksametanan A,Phondee N,et al.ADAMTSL1 and mandibular prognathism[J],Clinical Genetics,2019,95(4):507-515.
|
| [20] |
Rao CB,Guan BY,Luo D,et al.Identification of pathogenic variants of ERLEC1 in individuals with Class III malocclusion by exome sequencing[J].Human Mutation,2020,January:1-12.
|
| [21] |
Xiong XY,Li SY,Cai Y,et al.Targeted sequencing in FGF/FGFR genes and association analysis of variants for mandibular prognathism[J].Medicine (United States),2017,96:25.
|
| [22] |
Bayram S,Basciftci FA,Kurar E.Relationship between P561T and C422F polymorphisms in growth hormone receptor gene and mandibular prognathism[J].Angle Orthodontist,2014,83(5):803-809.
|
| [23] |
Saito F, Kajii TS, Oka A, et al.Genome-wide asso- ciation study for mandibular prognathism using microsatellite and pooled DNA method[J]. Am J Orthod Dentofacial Orthop,2017,152(3): 382-388.
|
| [24] |
Kajii TS,Oka A,Hatta M,et al.PLXNA2 identified as a candidate gene by genome-wide association analysis for mandibular prognathism in human chondrocytes[J].Biomedical Reports,2018,9(3):253-258.
|
| [25] |
Cruz CV,Mattos CT,Maia JC,et al.Genetic polymorphisms underlying the skeletal Class Ⅲ phenotype[J].American Journal of Orthodontics and Dentofacial Orthopedics,2017,151(4):700-707.
|
| [26] |
da Fontoura CS, Miller SF, Wehby GL, et al. Candidate Gene Analyses of Skeletal Variation in Malocclusion. J Dent Res. 2015;94(7):913-920.
|
| [27] |
Souza ND, Chalakkal P, Martires S,et al.Oral Manifestations of Nance-Horan Syndrome: A Report of a Rare Case[J].Contemp Clin Dent,2019,10(1):174-177.
|
| [28] |
Retrouvey JM,Taqi D,Tamimi F,et al.Oro-dental and cranio-facial characteristics of osteogenesis imperfecta type V[J].European Journal of Medical Genetics,2019,62(12):103606.
|
| [29] |
Bayram M,Yildirim M,Seymen F.Clinical and oral findings of a patient with Simpson–Golabi–Behmel syndrome[J].European Archives of Paediatric Dentistry,2014,16(1):63-66.
|
