Amelogenesis imperfecta (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Amelogenesis imperfecta" in English language version.

refsWebsite

Global rank English rank

39nih.gov

4^th place

23doi.org

2^nd place

2ljmu.ac.uk

low place

8,709^th place

2harvard.edu

18^th place

17^th place

2semanticscholar.org

11^th place

8^th place

2worldcat.org

5^th place

1books.google.com

3^rd place

1aapd.org

low place

aapd.org

American Academy of Pediatric Dentistry, Guideline on Dental Management of Heritable Dental Developmental Anomalies, 2013, http://www.aapd.org/media/Policies_Guidelines/G_OHCHeritable.pdf

books.google.com

Slootweg PJ (2007). Dental pathology: a practical introduction. Springer Science & Business Media. pp. 19–. ISBN 978-3-540-71690-7. Retrieved 28 December 2010.

doi.org

Kida M, Ariga T, Shirakawa T, Oguchi H, Sakiyama Y (November 2002). "Autosomal-dominant hypoplastic form of amelogenesis imperfecta caused by an enamelin gene mutation at the exon-intron boundary". Journal of Dental Research. 81 (11): 738–42. doi:10.1177/154405910208101103. PMID 12407086.
Smith CE, Murillo G, Brookes SJ, Poulter JA, Silva S, Kirkham J, Inglehearn CF, Mighell AJ (August 2016). "Deletion of amelotin exons 3-6 is associated with amelogenesis imperfecta". Human Molecular Genetics. 25 (16): 3578–3587. doi:10.1093/hmg/ddw203. PMC 5179951. PMID 27412008.
Crawford PJ, Aldred M, Bloch-Zupan A (April 2007). "Amelogenesis imperfecta". Orphanet Journal of Rare Diseases. 2 (1): 17. doi:10.1186/1750-1172-2-17. PMC 1853073. PMID 17408482.
Towle, Ian; Irish, Joel D. (2019). "A probable genetic origin for pitting enamel hypoplasia on the molars of Paranthropus robustus" (PDF). Journal of Human Evolution. 129: 54–61. Bibcode:2019JHumE.129...54T. doi:10.1016/j.jhevol.2019.01.002. PMID 30904040. S2CID 85502058.
Lagerström M, Dahl N, Nakahori Y, Nakagome Y, Bäckman B, Landegren U, Pettersson U (August 1991). "A deletion in the amelogenin gene (AMG) causes X-linked amelogenesis imperfecta (AIH1)". Genomics. 10 (4): 971–5. doi:10.1016/0888-7543(91)90187-j. PMID 1916828.
Rajpar MH, Harley K, Laing C, Davies RM, Dixon MJ (August 2001). "Mutation of the gene encoding the enamel-specific protein, enamelin, causes autosomal-dominant amelogenesis imperfecta". Human Molecular Genetics. 10 (16): 1673–7. doi:10.1093/hmg/10.16.1673. PMID 11487571.
Kim, Y. J.; Lee, Y.; Kasimoglu, Y.; Seymen, F.; Simmer, J. P.; Hu, J. C.-C.; Cho, E.-S.; Kim, J.-W. (January 2022). "Recessive Mutations in ACP4 Cause Amelogenesis Imperfecta". Journal of Dental Research. 101 (1): 37–45. doi:10.1177/00220345211015119. ISSN 1544-0591. PMC 8721729. PMID 34036831.
Kim JW, Simmer JP, Hart TC, Hart PS, Ramaswami MD, Bartlett JD, Hu JC (March 2005). "MMP-20 mutation in autosomal recessive pigmented hypomaturation amelogenesis imperfecta". Journal of Medical Genetics. 42 (3): 271–5. doi:10.1136/jmg.2004.024505. PMC 1736010. PMID 15744043.
Hart PS, Hart TC, Michalec MD, Ryu OH, Simmons D, Hong S, Wright JT (July 2004). "Mutation in kallikrein 4 causes autosomal recessive hypomaturation amelogenesis imperfecta". Journal of Medical Genetics. 41 (7): 545–9. doi:10.1136/jmg.2003.017657. PMC 1735847. PMID 15235027.
Kim JW, Lee SK, Lee ZH, Park JC, Lee KE, Lee MH, Park JT, Seo BM, Hu JC, Simmer JP (February 2008). "FAM83H mutations in families with autosomal-dominant hypocalcified amelogenesis imperfecta". American Journal of Human Genetics. 82 (2): 489–94. doi:10.1016/j.ajhg.2007.09.020. PMC 2427219. PMID 18252228.
El-Sayed W, Parry DA, Shore RC, Ahmed M, Jafri H, Rashid Y, et al. (November 2009). "Mutations in the beta propeller WDR72 cause autosomal-recessive hypomaturation amelogenesis imperfecta". American Journal of Human Genetics. 85 (5): 699–705. doi:10.1016/j.ajhg.2009.09.014. PMC 2775821. PMID 19853237.
Parry DA, Brookes SJ, Logan CV, Poulter JA, El-Sayed W, Al-Bahlani S, Al Harasi S, Sayed J, el Raïf M, Shore RC, Dashash M, Barron M, Morgan JE, Carr IM, Taylor GR, Johnson CA, Aldred MJ, Dixon MJ, Wright JT, Kirkham J, Inglehearn CF, Mighell AJ (September 2012). "Mutations in C4orf26, encoding a peptide with in vitro hydroxyapatite crystal nucleation and growth activity, cause amelogenesis imperfecta". American Journal of Human Genetics. 91 (3): 565–71. doi:10.1016/j.ajhg.2012.07.020. PMC 3511980. PMID 22901946.
Parry DA, Poulter JA, Logan CV, Brookes SJ, Jafri H, Ferguson CH, et al. (February 2013). "Identification of mutations in SLC24A4, encoding a potassium-dependent sodium/calcium exchanger, as a cause of amelogenesis imperfecta". American Journal of Human Genetics. 92 (2): 307–12. doi:10.1016/j.ajhg.2013.01.003. PMC 3567274. PMID 23375655.
Herzog CR, Reid BM, Seymen F, Koruyucu M, Tuna EB, Simmer JP, Hu JC (February 2015). "Hypomaturation amelogenesis imperfecta caused by a novel SLC24A4 mutation". Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology. 119 (2): e77–81. doi:10.1016/j.oooo.2014.09.003. PMC 4291293. PMID 25442250.
Poulter JA, El-Sayed W, Shore RC, Kirkham J, Inglehearn CF, Mighell AJ (January 2014). "Whole-exome sequencing, without prior linkage, identifies a mutation in LAMB3 as a cause of dominant hypoplastic amelogenesis imperfecta". European Journal of Human Genetics. 22 (1): 132–5. doi:10.1038/ejhg.2013.76. PMC 3865405. PMID 23632796.
Wang SK, Choi M, Richardson AS, Reid BM, Lin BP, Wang SJ, Kim JW, Simmer JP, Hu JC (April 2014). "ITGB6 loss-of-function mutations cause autosomal recessive amelogenesis imperfecta". Human Molecular Genetics. 23 (8): 2157–63. doi:10.1093/hmg/ddt611. PMC 3959820. PMID 24305999.
Visram S, McKaig S (December 2006). "Amelogenesis imperfecta--clinical presentation and management: a case report". Dental Update. 33 (10): 612–4, 616. doi:10.12968/denu.2006.33.10.612. PMID 17209536.
Crawford PJ, Aldred M, Bloch-Zupan A (April 2007). "Amelogenesis imperfecta". Orphanet Journal of Rare Diseases. 2: 17. doi:10.1186/1750-1172-2-17. PMC 1853073. PMID 17408482.
Sundell, S.; Valentin, J. (August 1986). "Hereditary aspects and classification of hereditary amelogenesis imperfecta". Community Dentistry and Oral Epidemiology. 14 (4): 211–216. doi:10.1111/j.1600-0528.1986.tb01537.x. ISSN 0301-5661. PMID 3461907.
Hoppenreijs TJ, Voorsmit RA, Freihofer HP (August 1998). "Open bite deformity in amelogenesis imperfecta. Part 1: An analysis of contributory factors and implications for treatment". Journal of Cranio-Maxillo-Facial Surgery. 26 (4): 260–6. doi:10.1016/s1010-5182(98)80023-1. PMID 9777506.
Towle I, Irish JD, De Groote I (April 2018). "Amelogenesis imperfecta in the dentition of a wild chimpanzee" (PDF). Journal of Medical Primatology. 47 (2): 117–119. doi:10.1111/jmp.12323. PMID 29112236. S2CID 3801451.
Chaudhary M, Dixit S, Singh A, Kunte S (July 2009). "Amelogenesis imperfecta: Report of a case and review of literature". Journal of Oral and Maxillofacial Pathology. 13 (2): 70–7. doi:10.4103/0973-029X.57673. PMC 3162864. PMID 21887005.
Hu JC, Chan HC, Simmer SG, Seymen F, Richardson AS, Hu Y, Milkovich RN, Estrella NM, Yildirim M, Bayram M, Chen CF, Simmer JP (2012). "Amelogenesis imperfecta in two families with defined AMELX deletions in ARHGAP6". PLOS ONE. 7 (12): e52052. Bibcode:2012PLoSO...752052H. doi:10.1371/journal.pone.0052052. PMC 3522662. PMID 23251683.

harvard.edu

ui.adsabs.harvard.edu

Towle, Ian; Irish, Joel D. (2019). "A probable genetic origin for pitting enamel hypoplasia on the molars of Paranthropus robustus" (PDF). Journal of Human Evolution. 129: 54–61. Bibcode:2019JHumE.129...54T. doi:10.1016/j.jhevol.2019.01.002. PMID 30904040. S2CID 85502058.
Hu JC, Chan HC, Simmer SG, Seymen F, Richardson AS, Hu Y, Milkovich RN, Estrella NM, Yildirim M, Bayram M, Chen CF, Simmer JP (2012). "Amelogenesis imperfecta in two families with defined AMELX deletions in ARHGAP6". PLOS ONE. 7 (12): e52052. Bibcode:2012PLoSO...752052H. doi:10.1371/journal.pone.0052052. PMC 3522662. PMID 23251683.

ljmu.ac.uk

researchonline.ljmu.ac.uk

Towle, Ian; Irish, Joel D. (2019). "A probable genetic origin for pitting enamel hypoplasia on the molars of Paranthropus robustus" (PDF). Journal of Human Evolution. 129: 54–61. Bibcode:2019JHumE.129...54T. doi:10.1016/j.jhevol.2019.01.002. PMID 30904040. S2CID 85502058.
Towle I, Irish JD, De Groote I (April 2018). "Amelogenesis imperfecta in the dentition of a wild chimpanzee" (PDF). Journal of Medical Primatology. 47 (2): 117–119. doi:10.1111/jmp.12323. PMID 29112236. S2CID 3801451.

nih.gov

pubmed.ncbi.nlm.nih.gov

Kida M, Ariga T, Shirakawa T, Oguchi H, Sakiyama Y (November 2002). "Autosomal-dominant hypoplastic form of amelogenesis imperfecta caused by an enamelin gene mutation at the exon-intron boundary". Journal of Dental Research. 81 (11): 738–42. doi:10.1177/154405910208101103. PMID 12407086.
Smith CE, Murillo G, Brookes SJ, Poulter JA, Silva S, Kirkham J, Inglehearn CF, Mighell AJ (August 2016). "Deletion of amelotin exons 3-6 is associated with amelogenesis imperfecta". Human Molecular Genetics. 25 (16): 3578–3587. doi:10.1093/hmg/ddw203. PMC 5179951. PMID 27412008.
Crawford PJ, Aldred M, Bloch-Zupan A (April 2007). "Amelogenesis imperfecta". Orphanet Journal of Rare Diseases. 2 (1): 17. doi:10.1186/1750-1172-2-17. PMC 1853073. PMID 17408482.
Towle, Ian; Irish, Joel D. (2019). "A probable genetic origin for pitting enamel hypoplasia on the molars of Paranthropus robustus" (PDF). Journal of Human Evolution. 129: 54–61. Bibcode:2019JHumE.129...54T. doi:10.1016/j.jhevol.2019.01.002. PMID 30904040. S2CID 85502058.
Lagerström M, Dahl N, Nakahori Y, Nakagome Y, Bäckman B, Landegren U, Pettersson U (August 1991). "A deletion in the amelogenin gene (AMG) causes X-linked amelogenesis imperfecta (AIH1)". Genomics. 10 (4): 971–5. doi:10.1016/0888-7543(91)90187-j. PMID 1916828.
Rajpar MH, Harley K, Laing C, Davies RM, Dixon MJ (August 2001). "Mutation of the gene encoding the enamel-specific protein, enamelin, causes autosomal-dominant amelogenesis imperfecta". Human Molecular Genetics. 10 (16): 1673–7. doi:10.1093/hmg/10.16.1673. PMID 11487571.
Kim, Y. J.; Lee, Y.; Kasimoglu, Y.; Seymen, F.; Simmer, J. P.; Hu, J. C.-C.; Cho, E.-S.; Kim, J.-W. (January 2022). "Recessive Mutations in ACP4 Cause Amelogenesis Imperfecta". Journal of Dental Research. 101 (1): 37–45. doi:10.1177/00220345211015119. ISSN 1544-0591. PMC 8721729. PMID 34036831.
Kim JW, Simmer JP, Hart TC, Hart PS, Ramaswami MD, Bartlett JD, Hu JC (March 2005). "MMP-20 mutation in autosomal recessive pigmented hypomaturation amelogenesis imperfecta". Journal of Medical Genetics. 42 (3): 271–5. doi:10.1136/jmg.2004.024505. PMC 1736010. PMID 15744043.
Hart PS, Hart TC, Michalec MD, Ryu OH, Simmons D, Hong S, Wright JT (July 2004). "Mutation in kallikrein 4 causes autosomal recessive hypomaturation amelogenesis imperfecta". Journal of Medical Genetics. 41 (7): 545–9. doi:10.1136/jmg.2003.017657. PMC 1735847. PMID 15235027.
Kim JW, Lee SK, Lee ZH, Park JC, Lee KE, Lee MH, Park JT, Seo BM, Hu JC, Simmer JP (February 2008). "FAM83H mutations in families with autosomal-dominant hypocalcified amelogenesis imperfecta". American Journal of Human Genetics. 82 (2): 489–94. doi:10.1016/j.ajhg.2007.09.020. PMC 2427219. PMID 18252228.
El-Sayed W, Parry DA, Shore RC, Ahmed M, Jafri H, Rashid Y, et al. (November 2009). "Mutations in the beta propeller WDR72 cause autosomal-recessive hypomaturation amelogenesis imperfecta". American Journal of Human Genetics. 85 (5): 699–705. doi:10.1016/j.ajhg.2009.09.014. PMC 2775821. PMID 19853237.
Parry DA, Brookes SJ, Logan CV, Poulter JA, El-Sayed W, Al-Bahlani S, Al Harasi S, Sayed J, el Raïf M, Shore RC, Dashash M, Barron M, Morgan JE, Carr IM, Taylor GR, Johnson CA, Aldred MJ, Dixon MJ, Wright JT, Kirkham J, Inglehearn CF, Mighell AJ (September 2012). "Mutations in C4orf26, encoding a peptide with in vitro hydroxyapatite crystal nucleation and growth activity, cause amelogenesis imperfecta". American Journal of Human Genetics. 91 (3): 565–71. doi:10.1016/j.ajhg.2012.07.020. PMC 3511980. PMID 22901946.
Parry DA, Poulter JA, Logan CV, Brookes SJ, Jafri H, Ferguson CH, et al. (February 2013). "Identification of mutations in SLC24A4, encoding a potassium-dependent sodium/calcium exchanger, as a cause of amelogenesis imperfecta". American Journal of Human Genetics. 92 (2): 307–12. doi:10.1016/j.ajhg.2013.01.003. PMC 3567274. PMID 23375655.
Herzog CR, Reid BM, Seymen F, Koruyucu M, Tuna EB, Simmer JP, Hu JC (February 2015). "Hypomaturation amelogenesis imperfecta caused by a novel SLC24A4 mutation". Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology. 119 (2): e77–81. doi:10.1016/j.oooo.2014.09.003. PMC 4291293. PMID 25442250.
Poulter JA, El-Sayed W, Shore RC, Kirkham J, Inglehearn CF, Mighell AJ (January 2014). "Whole-exome sequencing, without prior linkage, identifies a mutation in LAMB3 as a cause of dominant hypoplastic amelogenesis imperfecta". European Journal of Human Genetics. 22 (1): 132–5. doi:10.1038/ejhg.2013.76. PMC 3865405. PMID 23632796.
Wang SK, Choi M, Richardson AS, Reid BM, Lin BP, Wang SJ, Kim JW, Simmer JP, Hu JC (April 2014). "ITGB6 loss-of-function mutations cause autosomal recessive amelogenesis imperfecta". Human Molecular Genetics. 23 (8): 2157–63. doi:10.1093/hmg/ddt611. PMC 3959820. PMID 24305999.
Visram S, McKaig S (December 2006). "Amelogenesis imperfecta--clinical presentation and management: a case report". Dental Update. 33 (10): 612–4, 616. doi:10.12968/denu.2006.33.10.612. PMID 17209536.
Bouvier D, Duprez JP, Bois D (1996). "Rehabilitation of young patients with amelogenesis imperfecta: a report of two cases". ASDC Journal of Dentistry for Children. 63 (6): 443–7. PMID 9017180.
Crawford PJ, Aldred M, Bloch-Zupan A (April 2007). "Amelogenesis imperfecta". Orphanet Journal of Rare Diseases. 2: 17. doi:10.1186/1750-1172-2-17. PMC 1853073. PMID 17408482.
Sundell, S.; Valentin, J. (August 1986). "Hereditary aspects and classification of hereditary amelogenesis imperfecta". Community Dentistry and Oral Epidemiology. 14 (4): 211–216. doi:10.1111/j.1600-0528.1986.tb01537.x. ISSN 0301-5661. PMID 3461907.
Hoppenreijs TJ, Voorsmit RA, Freihofer HP (August 1998). "Open bite deformity in amelogenesis imperfecta. Part 1: An analysis of contributory factors and implications for treatment". Journal of Cranio-Maxillo-Facial Surgery. 26 (4): 260–6. doi:10.1016/s1010-5182(98)80023-1. PMID 9777506.
Towle I, Irish JD, De Groote I (April 2018). "Amelogenesis imperfecta in the dentition of a wild chimpanzee" (PDF). Journal of Medical Primatology. 47 (2): 117–119. doi:10.1111/jmp.12323. PMID 29112236. S2CID 3801451.
Chaudhary M, Dixit S, Singh A, Kunte S (July 2009). "Amelogenesis imperfecta: Report of a case and review of literature". Journal of Oral and Maxillofacial Pathology. 13 (2): 70–7. doi:10.4103/0973-029X.57673. PMC 3162864. PMID 21887005.
Hu JC, Chan HC, Simmer SG, Seymen F, Richardson AS, Hu Y, Milkovich RN, Estrella NM, Yildirim M, Bayram M, Chen CF, Simmer JP (2012). "Amelogenesis imperfecta in two families with defined AMELX deletions in ARHGAP6". PLOS ONE. 7 (12): e52052. Bibcode:2012PLoSO...752052H. doi:10.1371/journal.pone.0052052. PMC 3522662. PMID 23251683.

ncbi.nlm.nih.gov

Smith CE, Murillo G, Brookes SJ, Poulter JA, Silva S, Kirkham J, Inglehearn CF, Mighell AJ (August 2016). "Deletion of amelotin exons 3-6 is associated with amelogenesis imperfecta". Human Molecular Genetics. 25 (16): 3578–3587. doi:10.1093/hmg/ddw203. PMC 5179951. PMID 27412008.
Crawford PJ, Aldred M, Bloch-Zupan A (April 2007). "Amelogenesis imperfecta". Orphanet Journal of Rare Diseases. 2 (1): 17. doi:10.1186/1750-1172-2-17. PMC 1853073. PMID 17408482.
Kim, Y. J.; Lee, Y.; Kasimoglu, Y.; Seymen, F.; Simmer, J. P.; Hu, J. C.-C.; Cho, E.-S.; Kim, J.-W. (January 2022). "Recessive Mutations in ACP4 Cause Amelogenesis Imperfecta". Journal of Dental Research. 101 (1): 37–45. doi:10.1177/00220345211015119. ISSN 1544-0591. PMC 8721729. PMID 34036831.
Kim JW, Simmer JP, Hart TC, Hart PS, Ramaswami MD, Bartlett JD, Hu JC (March 2005). "MMP-20 mutation in autosomal recessive pigmented hypomaturation amelogenesis imperfecta". Journal of Medical Genetics. 42 (3): 271–5. doi:10.1136/jmg.2004.024505. PMC 1736010. PMID 15744043.
Hart PS, Hart TC, Michalec MD, Ryu OH, Simmons D, Hong S, Wright JT (July 2004). "Mutation in kallikrein 4 causes autosomal recessive hypomaturation amelogenesis imperfecta". Journal of Medical Genetics. 41 (7): 545–9. doi:10.1136/jmg.2003.017657. PMC 1735847. PMID 15235027.
Kim JW, Lee SK, Lee ZH, Park JC, Lee KE, Lee MH, Park JT, Seo BM, Hu JC, Simmer JP (February 2008). "FAM83H mutations in families with autosomal-dominant hypocalcified amelogenesis imperfecta". American Journal of Human Genetics. 82 (2): 489–94. doi:10.1016/j.ajhg.2007.09.020. PMC 2427219. PMID 18252228.
El-Sayed W, Parry DA, Shore RC, Ahmed M, Jafri H, Rashid Y, et al. (November 2009). "Mutations in the beta propeller WDR72 cause autosomal-recessive hypomaturation amelogenesis imperfecta". American Journal of Human Genetics. 85 (5): 699–705. doi:10.1016/j.ajhg.2009.09.014. PMC 2775821. PMID 19853237.
Parry DA, Brookes SJ, Logan CV, Poulter JA, El-Sayed W, Al-Bahlani S, Al Harasi S, Sayed J, el Raïf M, Shore RC, Dashash M, Barron M, Morgan JE, Carr IM, Taylor GR, Johnson CA, Aldred MJ, Dixon MJ, Wright JT, Kirkham J, Inglehearn CF, Mighell AJ (September 2012). "Mutations in C4orf26, encoding a peptide with in vitro hydroxyapatite crystal nucleation and growth activity, cause amelogenesis imperfecta". American Journal of Human Genetics. 91 (3): 565–71. doi:10.1016/j.ajhg.2012.07.020. PMC 3511980. PMID 22901946.
Parry DA, Poulter JA, Logan CV, Brookes SJ, Jafri H, Ferguson CH, et al. (February 2013). "Identification of mutations in SLC24A4, encoding a potassium-dependent sodium/calcium exchanger, as a cause of amelogenesis imperfecta". American Journal of Human Genetics. 92 (2): 307–12. doi:10.1016/j.ajhg.2013.01.003. PMC 3567274. PMID 23375655.
Herzog CR, Reid BM, Seymen F, Koruyucu M, Tuna EB, Simmer JP, Hu JC (February 2015). "Hypomaturation amelogenesis imperfecta caused by a novel SLC24A4 mutation". Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology. 119 (2): e77–81. doi:10.1016/j.oooo.2014.09.003. PMC 4291293. PMID 25442250.
Poulter JA, El-Sayed W, Shore RC, Kirkham J, Inglehearn CF, Mighell AJ (January 2014). "Whole-exome sequencing, without prior linkage, identifies a mutation in LAMB3 as a cause of dominant hypoplastic amelogenesis imperfecta". European Journal of Human Genetics. 22 (1): 132–5. doi:10.1038/ejhg.2013.76. PMC 3865405. PMID 23632796.
Wang SK, Choi M, Richardson AS, Reid BM, Lin BP, Wang SJ, Kim JW, Simmer JP, Hu JC (April 2014). "ITGB6 loss-of-function mutations cause autosomal recessive amelogenesis imperfecta". Human Molecular Genetics. 23 (8): 2157–63. doi:10.1093/hmg/ddt611. PMC 3959820. PMID 24305999.
Crawford PJ, Aldred M, Bloch-Zupan A (April 2007). "Amelogenesis imperfecta". Orphanet Journal of Rare Diseases. 2: 17. doi:10.1186/1750-1172-2-17. PMC 1853073. PMID 17408482.
Chaudhary M, Dixit S, Singh A, Kunte S (July 2009). "Amelogenesis imperfecta: Report of a case and review of literature". Journal of Oral and Maxillofacial Pathology. 13 (2): 70–7. doi:10.4103/0973-029X.57673. PMC 3162864. PMID 21887005.
Hu JC, Chan HC, Simmer SG, Seymen F, Richardson AS, Hu Y, Milkovich RN, Estrella NM, Yildirim M, Bayram M, Chen CF, Simmer JP (2012). "Amelogenesis imperfecta in two families with defined AMELX deletions in ARHGAP6". PLOS ONE. 7 (12): e52052. Bibcode:2012PLoSO...752052H. doi:10.1371/journal.pone.0052052. PMC 3522662. PMID 23251683.

semanticscholar.org

api.semanticscholar.org

Towle, Ian; Irish, Joel D. (2019). "A probable genetic origin for pitting enamel hypoplasia on the molars of Paranthropus robustus" (PDF). Journal of Human Evolution. 129: 54–61. Bibcode:2019JHumE.129...54T. doi:10.1016/j.jhevol.2019.01.002. PMID 30904040. S2CID 85502058.
Towle I, Irish JD, De Groote I (April 2018). "Amelogenesis imperfecta in the dentition of a wild chimpanzee" (PDF). Journal of Medical Primatology. 47 (2): 117–119. doi:10.1111/jmp.12323. PMID 29112236. S2CID 3801451.

worldcat.org

Kim, Y. J.; Lee, Y.; Kasimoglu, Y.; Seymen, F.; Simmer, J. P.; Hu, J. C.-C.; Cho, E.-S.; Kim, J.-W. (January 2022). "Recessive Mutations in ACP4 Cause Amelogenesis Imperfecta". Journal of Dental Research. 101 (1): 37–45. doi:10.1177/00220345211015119. ISSN 1544-0591. PMC 8721729. PMID 34036831.
Sundell, S.; Valentin, J. (August 1986). "Hereditary aspects and classification of hereditary amelogenesis imperfecta". Community Dentistry and Oral Epidemiology. 14 (4): 211–216. doi:10.1111/j.1600-0528.1986.tb01537.x. ISSN 0301-5661. PMID 3461907.