Below are the most recent publications written about "Tooth Abnormalities" by people in Profiles.
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Doolan BJ, Onoufriadis A, Kantaputra P, McGrath JA. WNT10A, dermatology and dentistry. Br J Dermatol. 2021 12; 185(6):1105-1111.
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Strauss KA, Jinks RN, Puffenberger EG, Venkatesh S, Singh K, Cheng I, Mikita N, Thilagavathi J, Lee J, Sarafianos S, Benkert A, Koehler A, Zhu A, Trovillion V, McGlincy M, Morlet T, Deardorff M, Innes AM, Prasad C, Chudley AE, Lee IN, Suzuki CK. CODAS syndrome is associated with mutations of LONP1, encoding mitochondrial AAA+ Lon protease. Am J Hum Genet. 2015 Jan 08; 96(1):121-35.
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Sulkowski JP, Cooper JN, Duggan EM, Balci O, Anandalwar S, Blakely ML, Heiss K, Rangel SJ, Minneci PC, Deans KJ. Early versus delayed surgical correction of malrotation in children with critical congenital heart disease. J Pediatr Surg. 2015 Jan; 50(1):86-91.
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Samaan G, Yugo D, Rajagopalan S, Wall J, Donnell R, Goldowitz D, Gopalakrishnan R, Venkatachalam S. Foxn3 is essential for craniofacial development in mice and a putative candidate involved in human congenital craniofacial defects. Biochem Biophys Res Commun. 2010 Sep 10; 400(1):60-5.
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Mahoney MG, Sadowski S, Brennan D, Pikander P, Saukko P, Wahl J, Aho H, Heikinheimo K, Bruckner-Tuderman L, Fertala A, Peltonen J, Uitto J, Peltonen S. Compound heterozygous desmoplakin mutations result in a phenotype with a combination of myocardial, skin, hair, and enamel abnormalities. J Invest Dermatol. 2010 Apr; 130(4):968-78.
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Zamiri M, McLean WH, Hodgins MB, Munro CS. Pachyonychia congenita type 2: abnormal dentition extending into adulthood. Br J Dermatol. 2008 Aug; 159(2):500-1.
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Vallino LD, Zuker R, Napoli JA. A study of speech, language, hearing, and dentition in children with cleft lip only. Cleft Palate Craniofac J. 2008 Sep; 45(5):485-94.
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Kelly SC, Ratajczak P, Keller M, Purcell SM, Griffin T, Richard G. A novel GJA 1 mutation in oculo-dento-digital dysplasia with curly hair and hyperkeratosis. Eur J Dermatol. 2006 May-Jun; 16(3):241-5.
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Chan I, Harper JI, Mellerio JE, McGrath JA. ADULT ectodermal dysplasia syndrome resulting from the missense mutation R298Q in the p63 gene. Clin Exp Dermatol. 2004 Nov; 29(6):669-72.
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Graubard SA. Fusion of a lower second and third molar and macrodontia of a lower first molar. Oral Surg Oral Med Oral Pathol. 1977 Nov; 44(5):817.