These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
3. Otodental syndrome. A case report. Van Doorne L; Wackens G; De Maeseneer M; Deron P Int J Oral Maxillofac Surg; 1998 Apr; 27(2):121-4. PubMed ID: 9565269 [TBL] [Abstract][Full Text] [Related]
4. "Otodental" dysplasia. Chen RJ; Chen HS; Lin LM; Lin CC; Jorgenson RJ Oral Surg Oral Med Oral Pathol; 1988 Sep; 66(3):353-8. PubMed ID: 3050710 [TBL] [Abstract][Full Text] [Related]
5. Autosomal dominant hypohidrotic ectodermal dysplasia in a large family. Aswegan AL; Josephson KD; Mowbray R; Pauli RM; Spritz RA; Williams MS Am J Med Genet; 1997 Nov; 72(4):462-7. PubMed ID: 9375732 [TBL] [Abstract][Full Text] [Related]
6. Otodental syndrome, oculo-facio-cardio-dental (OFCD) syndrome, and lobodontia: dental disorders of interest to the pediatric radiologist. Gorlin RJ Pediatr Radiol; 1998 Oct; 28(10):802-4. PubMed ID: 9799305 [TBL] [Abstract][Full Text] [Related]
7. Osteogenesis imperfecta type I with unusual dental abnormalities. Levin LS; Young RJ; Pyeritz RE Am J Med Genet; 1988 Dec; 31(4):921-32. PubMed ID: 3239581 [TBL] [Abstract][Full Text] [Related]
8. Abnormal primary and permanent dentitions with ectodermal symptoms predict WNT10A deficiency. Bergendal B; Norderyd J; Zhou X; Klar J; Dahl N BMC Med Genet; 2016 Nov; 17(1):88. PubMed ID: 27881089 [TBL] [Abstract][Full Text] [Related]
9. Otodental syndrome: a case report. Colter JD; Sedano HO Pediatr Dent; 2005; 27(6):482-5. PubMed ID: 16532889 [TBL] [Abstract][Full Text] [Related]
11. Oligodontia ectodermal dysplasia--on signs, symptoms, genetics, and outcomes of dental treatment. Bergendal B Swed Dent J Suppl; 2010; (205):13-78, 7-8. PubMed ID: 20626136 [TBL] [Abstract][Full Text] [Related]
12. Natal teeth and steatocystoma multiplex complicated by hidradenitis suppurativa. A new syndrome. McDonald RM; Reed WB Arch Dermatol; 1976 Aug; 112(8):1132-4. PubMed ID: 988984 [TBL] [Abstract][Full Text] [Related]
13. Dermoodontodysplasia: an eleven-member, four generation pedigree with an apparently hitherto undescribed pure ectodermal dysplasia. Pinheiro M; Freire-Maia N Clin Genet; 1983 Jul; 24(1):58-68. PubMed ID: 6616948 [TBL] [Abstract][Full Text] [Related]
15. A previously undescribed ectodermal dysplasia of the tricho-odonto-onychial subgroup in a family. Tsakalakos N; Jordaan FH; Taljaard JJ; Hough SF Arch Dermatol; 1986 Sep; 122(9):1047-53. PubMed ID: 3740884 [TBL] [Abstract][Full Text] [Related]
16. Cleft lip/palate-oligodontia-syndactyly-hair alterations, a new syndrome: review of the conditions combining ectodermal dysplasia and cleft lip/palate. MartÃnez B; Monasterio L; Pinheiro M; Freire-Maia N Am J Med Genet; 1987 May; 27(1):23-31. PubMed ID: 3037904 [TBL] [Abstract][Full Text] [Related]
17. [Dental anomalies in some hereditary syndromes observed by the authors]. Desiate A; Milano V Minerva Stomatol; 1998 Sep; 47(9):361-6. PubMed ID: 9835742 [TBL] [Abstract][Full Text] [Related]
18. Dental implications of Tooth-Nail dysplasia (Witkop syndrome): a report of an affected family and an approach to dental management. Wicomb GM; Stephen LX; Beighton P J Clin Pediatr Dent; 2004; 28(2):107-12. PubMed ID: 14969367 [TBL] [Abstract][Full Text] [Related]
19. Anomalies of tooth formation in hypohidrotic ectodermal dysplasia. Lexner MO; Bardow A; Hertz JM; Nielsen LA; Kreiborg S Int J Paediatr Dent; 2007 Jan; 17(1):10-8. PubMed ID: 17181574 [TBL] [Abstract][Full Text] [Related]
20. Brief clinical report: new, autosomal dominant form of ectodermal dysplasia. Tuffli GA; Laxova R Am J Med Genet; 1983 Feb; 14(2):381-4. PubMed ID: 6837633 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]