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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1993 1
1994 3
1995 3
1996 3
1997 4
1998 2
2000 1
2002 3
2003 1
2006 1
2009 4
2010 2
2011 3
2012 2
2013 3
2014 4
2015 5
2016 4
2017 6
2018 5
2019 2
2020 3
2021 2
2022 2
2023 2
2024 4

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68 results

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Page 1
Vertebrate pseudogenes.
Mighell AJ, Smith NR, Robinson PA, Markham AF. Mighell AJ, et al. FEBS Lett. 2000 Feb 25;468(2-3):109-14. doi: 10.1016/s0014-5793(00)01199-6. FEBS Lett. 2000. PMID: 10692568 Free article. Review.
Alu sequences.
Mighell AJ, Markham AF, Robinson PA. Mighell AJ, et al. FEBS Lett. 1997 Nov 3;417(1):1-5. doi: 10.1016/s0014-5793(97)01259-3. FEBS Lett. 1997. PMID: 9395063 Free article. Review.
Amelogenesis Imperfecta; Genes, Proteins, and Pathways.
Smith CEL, Poulter JA, Antanaviciute A, Kirkham J, Brookes SJ, Inglehearn CF, Mighell AJ. Smith CEL, et al. Among authors: mighell aj. Front Physiol. 2017 Jun 26;8:435. doi: 10.3389/fphys.2017.00435. eCollection 2017. Front Physiol. 2017. PMID: 28694781 Free PMC article. Review.
Novel Ameloblastin Variants, Contrasting Amelogenesis Imperfecta Phenotypes.
Hany U, Watson CM, Liu L, Nikolopoulos G, Smith CEL, Poulter JA, Brown CJ, Patel A, Rodd HD, Balmer R, Harfoush A, Al-Jawad M, Inglehearn CF, Mighell AJ. Hany U, et al. Among authors: mighell aj. J Dent Res. 2024 Jan;103(1):22-30. doi: 10.1177/00220345231203694. Epub 2023 Dec 6. J Dent Res. 2024. PMID: 38058155 Free PMC article.
Dentin dysplasia: diagnostic challenges.
Alhilou A, Beddis HP, Mighell AJ, Durey K. Alhilou A, et al. Among authors: mighell aj. BMJ Case Rep. 2018 Jun 11;2018:bcr2017223942. doi: 10.1136/bcr-2017-223942. BMJ Case Rep. 2018. PMID: 29895546 Free PMC article.
Heterozygous COL17A1 variants are a frequent cause of amelogenesis imperfecta.
Hany U, Watson CM, Liu L, Smith CEL, Harfoush A, Poulter JA, Nikolopoulos G, Balmer R, Brown CJ, Patel A, Simmonds J, Charlton R, Acosta de Camargo MG, Rodd HD, Jafri H, Antanaviciute A, Moffat M, Al-Jawad M, Inglehearn CF, Mighell AJ. Hany U, et al. Among authors: mighell aj. J Med Genet. 2024 Mar 21;61(4):347-355. doi: 10.1136/jmg-2023-109510. J Med Genet. 2024. PMID: 37979963 Free PMC article.
Biallelic variants in Plexin B2 (PLXNB2) cause amelogenesis imperfecta, hearing loss and intellectual disability.
Smith CEL, Laugel-Haushalter V, Hany U, Best S, Taylor RL, Poulter JA, Wortmann SB, Feichtinger RG, Mayr JA, Al Bahlani S, Nikolopoulos G, Rigby A, Black GC, Watson CM, Mansour S, Inglehearn CF, Mighell AJ, Bloch-Zupan A; UK Inherited Retinal Disease Consortium, Genomics England Research Consortium. Smith CEL, et al. Among authors: mighell aj. J Med Genet. 2024 Jun 20;61(7):689-698. doi: 10.1136/jmg-2023-109728. J Med Genet. 2024. PMID: 38458752 Free PMC article.
68 results