| 1 | FTA1, MSX1
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| MSX1 involved selective tooth agenesis and abnormal labial frenum, pedigree, and retrospective study.
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| Zhu Y, Zhang Y, Dong J, Ruan W, Yang S, Huang P, Duan X.
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| Oral Dis. Dec 7. doi: 10.1111/odi.14459. Epub ahead of print. 2022
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| 2 | FTA1, MSX1, OLD, PAX9
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| PAX9 and MSX1 transcription factor genes in non-syndromic dental agenesis.
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| Paixão-Côrtes VR, Braga T, Salzano FM, Mundstock K, Mundstock CA, Bortolini MC.
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| Arch Oral Biol 56(4):337-44. Epub 2010 Dec 15.
2011
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| 3 | FTA1, MSX1, OLD, PAX9
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| Mutational analysis of MSX1 and PAX9 genes in Portuguese families with maxillary lateral incisor agenesis.
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| Pinho T, Silva-Fernandes A, Bousbaa H, Maciel P.
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| Eur J Orthod 32(5):582-8. Epub 2010 Jul 26.
2010
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| 4 | AI1C, AIH1, AIH2, AIH3, AIHHT, AIPH1, AIPH2, AMELX, AXIN1, DD2, DGI1, DLX3, DSPP, ENAM, FTA1, FTACC, KLK4, MMP20, MSX1, OLD, PAX9, STHAG5, ZNF22
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| The genetic basis of inherited anomalies of the teeth. Part 1: clinical and molecular aspects of non-syndromic dental disorders.
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| Bailleul-Forestier I, Molla M, Verloes A, Berdal A.
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| Eur J Med Genet 51(4):273-91. Epub 2008 Mar 26. Review.
2008
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| 5 | MSX1, FTA1
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| A novel MSX1 mutation in hypodontia.
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| De Muynck S, Schollen E, Matthijs G, Verdonck A, Devriendt K, Carels C.
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| Am J Med Genet 128A(4):401-3. 2004
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| 6 | FTA1, MSX1, OFC5
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| Complete sequencing shows a role for MSX1 in non-syndromic cleft lip and palate.
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| Jezewski PA, Vieira AR, Nishimura C, Ludwig B, Johnson M, O'Brien SE, Daack-Hirsch S, Schultz RE, Weber A, Nepomucena B, Romitti PA, Christensen K, Orioli IM, Castilla EE, Machida J, Natsume N, Murray JC.
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| J Med Genet 40(6):399-407. 2003
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| 7 | FTA1, MSX1
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| A nonsense mutation in MSX1 causes Witkop syndrome.
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| Jumlongras D, Bei M, Stimson JM, Wang WF, DePalma SR, Seidman CE, Felbor U, Maas R, Seidman JG, Olsen BR.
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| Am J Hum Genet 69(1):67-74. 2001
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| 8 | FTA1, MSX1, OFC5
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| MSX1 mutation is associated with orofacial clefting and tooth agenesis in humans.
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| van den Boogaard MJ, Dorland M, Beemer FA, van Amstel HK.
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| Nat Genet 24(4):342-3. 2000
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| 9 | FTA1, MSX1
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| Absence of mutations in the homeodomain of the MSX1 gene in patients with hypodontia.
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| Scarel RM, Trevilatto PC, Di Hipolito O Jr, Camargo LE, Line SR.
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| Am J Med Genet 92(5):346-9. 2000
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| 10 | FTA1, MSX1
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| A human MSX1 homeodomain missense mutation causes selective tooth agenesis.
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| Vastardis H, et al.
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| Nat Genet 13 : 417-422. 1996
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