182 related articles for article (PubMed ID: 29554435)
21. Amelogenesis imperfecta due to a mutation of the enamelin gene: clinical case with genotype-phenotype correlations.
Lindemeyer RG; Gibson CW; Wright TJ
Pediatr Dent; 2010; 32(1):56-60. PubMed ID: 20298654
[TBL] [Abstract][Full Text] [Related]
22. Alteration of Exon Definition Causes Amelogenesis Imperfecta.
Kim YJ; Kang J; Seymen F; Koruyucu M; Zhang H; Kasimoglu Y; Bayram M; Tuna-Ince EB; Bayrak S; Tuloglu N; Hu JC; Simmer JP; Kim JW
J Dent Res; 2020 Apr; 99(4):410-418. PubMed ID: 31999931
[TBL] [Abstract][Full Text] [Related]
23. Phenotypic variability in LAMA3-associated amelogenesis imperfecta.
Wang SK; Zhang H; Wang YL; Seymen F; Koruyucu M; Simmer JP; Hu JC
Oral Dis; 2023 Nov; 29(8):3514-3524. PubMed ID: 36326426
[TBL] [Abstract][Full Text] [Related]
24. Candidate gene sequencing reveals mutations causing hypoplastic amelogenesis imperfecta.
Kim YJ; Seymen F; Kang J; Koruyucu M; Tuloglu N; Bayrak S; Tuna EB; Lee ZH; Shin TJ; Hyun HK; Kim YJ; Lee SH; Hu J; Simmer J; Kim JW
Clin Oral Investig; 2019 Mar; 23(3):1481-1487. PubMed ID: 30120606
[TBL] [Abstract][Full Text] [Related]
25. Craniofacial characteristics and genotypes of amelogenesis imperfecta patients.
Pavlic A; Battelino T; Trebusak Podkrajsek K; Ovsenik M
Eur J Orthod; 2011 Jun; 33(3):325-31. PubMed ID: 21068190
[TBL] [Abstract][Full Text] [Related]
26. Recessive Mutations in ACPT, Encoding Testicular Acid Phosphatase, Cause Hypoplastic Amelogenesis Imperfecta.
Seymen F; Kim YJ; Lee YJ; Kang J; Kim TH; Choi H; Koruyucu M; Kasimoglu Y; Tuna EB; Gencay K; Shin TJ; Hyun HK; Kim YJ; Lee SH; Lee ZH; Zhang H; Hu JC; Simmer JP; Cho ES; Kim JW
Am J Hum Genet; 2016 Nov; 99(5):1199-1205. PubMed ID: 27843125
[TBL] [Abstract][Full Text] [Related]
27. Amelogenesis Imperfecta: 1 Family, 2 Phenotypes, and 2 Mutated Genes.
Prasad MK; Laouina S; El Alloussi M; Dollfus H; Bloch-Zupan A
J Dent Res; 2016 Dec; 95(13):1457-1463. PubMed ID: 27558265
[TBL] [Abstract][Full Text] [Related]
28. Digenic inheritance accounts for phenotypic variability in amelogenesis imperfecta.
Yang Y; Qin M; Zhao Y; Wang X
Clin Genet; 2024 Mar; 105(3):243-253. PubMed ID: 37937686
[TBL] [Abstract][Full Text] [Related]
29. Mutations in RELT cause autosomal recessive amelogenesis imperfecta.
Kim JW; Zhang H; Seymen F; Koruyucu M; Hu Y; Kang J; Kim YJ; Ikeda A; Kasimoglu Y; Bayram M; Zhang C; Kawasaki K; Bartlett JD; Saunders TL; Simmer JP; Hu JC
Clin Genet; 2019 Mar; 95(3):375-383. PubMed ID: 30506946
[TBL] [Abstract][Full Text] [Related]
30. ITGB6 loss-of-function mutations cause autosomal recessive amelogenesis imperfecta.
Wang SK; Choi M; Richardson AS; Reid BM; Lin BP; Wang SJ; Kim JW; Simmer JP; Hu JC
Hum Mol Genet; 2014 Apr; 23(8):2157-63. PubMed ID: 24305999
[TBL] [Abstract][Full Text] [Related]
31. Whole exome sequencing identifies an AMBN missense mutation causing severe autosomal-dominant amelogenesis imperfecta and dentin disorders.
Lu T; Li M; Xu X; Xiong J; Huang C; Zhang X; Hu A; Peng L; Cai D; Zhang L; Wu B; Xiong F
Int J Oral Sci; 2018 Sep; 10(3):26. PubMed ID: 30174330
[TBL] [Abstract][Full Text] [Related]
32. Recessive Mutations in
Kim YJ; Lee Y; Kasimoglu Y; Seymen F; Simmer JP; Hu JC; Cho ES; Kim JW
J Dent Res; 2022 Jan; 101(1):37-45. PubMed ID: 34036831
[TBL] [Abstract][Full Text] [Related]
33. Enamelin and autosomal-dominant amelogenesis imperfecta.
Hu JC; Yamakoshi Y
Crit Rev Oral Biol Med; 2003; 14(6):387-98. PubMed ID: 14656895
[TBL] [Abstract][Full Text] [Related]
34. Mutations in the beta propeller WDR72 cause autosomal-recessive hypomaturation amelogenesis imperfecta.
El-Sayed W; Parry DA; Shore RC; Ahmed M; Jafri H; Rashid Y; Al-Bahlani S; Al Harasi S; Kirkham J; Inglehearn CF; Mighell AJ
Am J Hum Genet; 2009 Nov; 85(5):699-705. PubMed ID: 19853237
[TBL] [Abstract][Full Text] [Related]
35. A novel nonsense variant in SLC24A4 causing a rare form of amelogenesis imperfecta in a Pakistani family.
Khan SA; Khan MA; Muhammad N; Bashir H; Khan N; Muhammad N; Yilmaz R; Khan S; Wasif N
BMC Med Genet; 2020 May; 21(1):97. PubMed ID: 32380970
[TBL] [Abstract][Full Text] [Related]
36. Novel FAM20A mutation causes autosomal recessive amelogenesis imperfecta.
Volodarsky M; Zilberman U; Birk OS
Arch Oral Biol; 2015 Jun; 60(6):919-22. PubMed ID: 25827751
[TBL] [Abstract][Full Text] [Related]
37. Phenotype and Variant Spectrum in the LAMB3 Form of Amelogenesis Imperfecta.
Smith CEL; Poulter JA; Brookes SJ; Murillo G; Silva S; Brown CJ; Patel A; Hussain H; Kirkham J; Inglehearn CF; Mighell AJ
J Dent Res; 2019 Jun; 98(6):698-704. PubMed ID: 30905256
[TBL] [Abstract][Full Text] [Related]
38. Four novel mutations of FAM20A in amelogenesis imperfecta type IG and review of literature for its genotype and phenotype spectra.
Nitayavardhana I; Theerapanon T; Srichomthong C; Piwluang S; Wichadakul D; Porntaveetus T; Shotelersuk V
Mol Genet Genomics; 2020 Jul; 295(4):923-931. PubMed ID: 32246227
[TBL] [Abstract][Full Text] [Related]
39. Identification of the enamelin (g.8344delG) mutation in a new kindred and presentation of a standardized ENAM nomenclature.
Hart PS; Michalec MD; Seow WK; Hart TC; Wright JT
Arch Oral Biol; 2003 Aug; 48(8):589-96. PubMed ID: 12828988
[TBL] [Abstract][Full Text] [Related]
40. The structure and composition of deciduous enamel affected by local hypoplastic autosomal dominant amelogenesis imperfecta resulting from an ENAM mutation.
Shore RC; Bäckman B; Elcock C; Brook AH; Brookes SJ; Kirkham J
Cells Tissues Organs; 2010; 191(4):301-6. PubMed ID: 19923784
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
