参考文献/References:
[1] CHEN F,LI Q,GU M,et al.Identification of a mutation in FGF23 involved in mandibular prognathism[J].Scientific Reports,2015(5):11250.
[2] JOSHI N,HAMDAN A M,FAKHOURI W D.Skeletal malocclusion:A developmental disorder with a life-long morbidity[J].Journal of Clinical Medicine Research,2014,6(6):399-408.
[3] DA-FONTOURA C S,MILLER S F,WEHBY G L,et al.Candidate gene analyses of skeletal variation in malocclusion[J].Journal of Dental Research,2015,94(7):913-920.
[4] 高宾,王春花,李雅琪,等.长链非编码RNA在口腔鳞状细胞癌中作用的研究进展[J].陕西医学杂志,2022,51(11):1458-1462.
[5] 高旭航,郑玉群,何志杰,等.基因多态性与糖尿病肾病关系研究进展[J].陕西医学杂志,2019,48(11):1574-1577.
[6] 王爽,丰培勋,郭雄,等.骨性安氏 Ⅲ 类错牙合的遗传度分析[J].上海口腔医学,2006,15(3):269.
[7] YAMAGUCHI T,PARK S B,NARITA A,et al.Genome-wide linkage analysis of mandibular prognathism in Korean and Japanese patients[J].Journal of Dental Research,2005,84(3):255-259.
[8] LI Q,LI X,ZHANG F,et al.The identification of a novel locus for mandibular prognathism in the Han Chinese population[J].Journal of Dental Research,2011,90(1):53-57.
[9] LI Q,ZHANG F,LI X,et al.Genome scan for locus involved in mandibular prognathism in pedigrees from China[J].PloS One,2010,5(9):e12678.
[10] CRUZ R M,HARTSFIELD J K,FALCAO-ALENCAR G,et al.Exclusion of class Ⅲ malocclusion candidate loci in Brazilian families[J].Journal of Dental Research,2011,90(10):1202-1205.
[11] NIKOPENSIUS T,SAAG M,JAGOMAG I T,et al.A missense mutation in DUSP6 is associated with class Ⅲ malocclusion[J].Journal of Dental Research,2013,92(10):893-898.
[12] GUAN X,SONG Y,OTT J,et al.The ADAMTS1 gene is associated with familial mandibular prognathism[J].Journal of Dental Research,2015,94(9):1196-1201.
[13] KAJII T S,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,2019,122:193-198.
[14] KANTAPUTRA P N,PRUKSAMETANAN A,PHONDEE N,et al.ADAMTSL1 and mandibular prognathism[J].Clinical Genetics,2019,95(4):507-515.
[15] RAO C,GUAN B,LUO D,et al.Identification of pathogenic variants of ERLEC1 in individuals with class Ⅲ malocclusion by exome sequencing[J].Human Mutation,2020,41(8):1435-1446.
[16] SUN F,WONG R,RABIE A B.Identification of SNP markers on 1p36 and association analysis of EPB41 with mandibular prognathism in a Chinese population[J].Archives of Oral Biology,2010,55(11):867-872.
[17] SUN F,RABIE A B,LUO G.Analysis of the association of COL2A1 and IGF-1 with mandibular prognathism in a Chinese population[J].Orthodontics & Craniofacial Research,2014,17(3):144-149.
[18] JANG J Y,PARK E K,RYOO H M,et al.Polymorphisms in the Matrilin-1 gene and risk of mandibular prognathism in Koreans[J].Journal of Dental Research,2010,89(11):1203-1207.
[19] TASSOPOULOU-FISHELL M,DEELEY K,HARVEY E M,et al.Genetic variation in myosin 1H contributes to mandibular prognathism[J].American Journal of Orthodontics and Dentofacial Orthopedics,2012,141(1):51-59.
[20] CRUZ C V,MATTOS C T,MAIA J C,et al.Genetic polymorphisms underlying the skeletal Class Ⅲ phenotype[J].American Journal of Orthodontics and Dentofacial Orthopedics,2017,151(4):700-707.
[21] SUN R,WANG Y,JIN M,et al.Identification and functional studies of MYO1H for mandibular prognathism[J].Journal of Dental Research,2018,97(13):1501-1509.
[22] BAYRAM S,BASCIFTCI F A,KURAR E.Relationship between P561T and C422F polymorphisms in growth hormone receptor gene and mandibular prognathism[J].The Angle Orthodontist,2014,84(5):803-809.
[23] TOBN-ARROYAVE S I,JIMNEZ-ARBELEZ G A,ALVARADO-GMEZ V A,et al.Association analysis between rs6184 and rs6180 polymorphisms of growth hormone receptor gene regarding skeletal-facial profile in a Colombian population[J].European Journal of Orthodontics,2018,40(4):378-386.
[24] IKUNO K,KAJII T S,OKA A,et al.Microsatellite genome-wide association study for mandibular prognathism[J].American Journal of Orthodontics and Dentofacial Orthopedics,2014,145(6):757-762.
[25] FRAZIER-BOWERS S,RINCON-RODRIGUEZ R,ZHOU J,et al.Evidence of linkage in a Hispanic cohort with a class Ⅲ dentofacial phenotype[J].Journal of Dental Research,2009,88(1):56-60.
[26] PERILLO L,MONSURRA,BONCI E,et al.Genetic association of ARHGAP21 gene variant with mandibular prognathism[J].Journal of Dental Research,2015,94(4):569-576.
[27] SAITO F,KAJII T S,OKA A,et al.Genome-wide association study for mandibular prognathism using microsatellite and pooled DNA method[J].American Journal of Orthodontics and Dentofacial Orthopedics,2017,152(3):382-388.
[28] XIONG X,LI S,CAI Y,et al.Targeted sequencing in FGF/FGFR genes and association analysis of variants for mandibular prognathism[J].Medicine,2017,96(25):e7240.
[29] HAN X,XIONG X,SHI X,et al.Targeted sequencing of NOTCH signaling pathway genes and association analysis of variants correlated with mandibular prognathism[J].Head & Face Medicine,2021,17(1):17.
[30] IAQUINTA M R,LANZILLOTTI C,MAZZIOTTA C,et al.The role of microRNAs in the osteogenic and chondrogenic differentiation of mesenchymal stem cells and bone pathologies[J].Theranostics,2021,11(13):6573-6591.
[31] GU Y,ZHANG Y,ZHAO C,et al.Serum microRNAs as potential biomarkers of mandibular prognathism[J].Oral Diseases,2014,20(1):55-61.
[32] TIAN Y,LIU J,BAI X,et al.MicroRNA expression profile of surgical removed mandibular bone tissues from patients with mandibular prognathism[J].The Journal of Surgical Research,2015,198(1):127-134.
[33] DE SOUZA N,CHALAKKAL P,MARTIRES S,et al.Oral manifestations of nance-horan syndrome:A report of a rare case[J].Contemporary Clinical Dentistry,2019,10(1):174-177.
[34] BAGATTONI S,D'ALESSANDRO G,SADOTTI A,et al.Oro-dental features of Pallister-Killian syndrome:Evaluation of 21 European probands[J].American Journal Of Medical Genetics Part A,2016,170(9):2357-2364.
[35] DU Q,ZHANG D,ZHUANG Y,et al.The molecular genetics of Marfan syndrome[J].International Journal of Medical Sciences,2021,18(13):2752.
[36] FEGHALI S,VI-FANE B,PICARD A,et al.Dental and orthodontic follow-up in nevoid basal cell carcinoma syndrome patient with odontogenic keratocystic tumors[J].Journal of Stomatology,Oral and Maxillofacial Surgery,2022,123(3):e57-e61.
[37] BAYRAM M,YILDIRIM M,SEYMEN F.Clinical and oral findings of a patient with Simpson-Golabi-Behmel syndrome[J].European Archives of Paediatric Dentistry:Official Journal of the European Academy of Paediatric Dentistry,2015,16(1):63-66.
[38] LIU H,WANG Y,LIU H,et al.Novel DLX3 variant identified in a family with tricho-dento-osseous syndrome[J].Archives of Oral Biology,2022,141:105479.