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.
23. Seckel syndrome: report of a case. Seymen F; Tuna B; Kayserili H J Clin Pediatr Dent; 2002; 26(3):305-9. PubMed ID: 11990056 [TBL] [Abstract][Full Text] [Related]
24. Microdontia, hypodontia, short bulbous roots and root canals with strabismus, short stature, and borderline mentality. Bazopoulou-Kyrkanidou E; Dacou-Voutetakis C; Nassi H; Tosios K; Kyrkanides S; Damoli M Oral Surg Oral Med Oral Pathol; 1992 Jul; 74(1):93-5. PubMed ID: 1508516 [TBL] [Abstract][Full Text] [Related]
25. A child with 18p- syndrome: a case report. Naudi AB; Fung DE Spec Care Dentist; 2007; 27(1):12-4. PubMed ID: 17388224 [TBL] [Abstract][Full Text] [Related]
26. Neurobehavioral phenotype observed in KBG syndrome caused by ANKRD11 mutations. Lo-Castro A; Brancati F; Digilio MC; Garaci FG; Bollero P; Alfieri P; Curatolo P Am J Med Genet B Neuropsychiatr Genet; 2013 Jan; 162B(1):17-23. PubMed ID: 23184435 [TBL] [Abstract][Full Text] [Related]
27. A maxillary central incisor having two root canals geminated with a supernumerary tooth. Hosomi T; Yoshikawa M; Yaoi M; Sakiyama Y; Toda T J Endod; 1989 Apr; 15(4):161-3. PubMed ID: 2607286 [TBL] [Abstract][Full Text] [Related]
28. The KBG syndrome: confirmation of autosomal dominant inheritance and further delineation of the phenotype. Tekin M; Kavaz A; Berberoğlu M; Fitoz S; Ekim M; Ocal G; Akar N Am J Med Genet A; 2004 Oct; 130A(3):284-7. PubMed ID: 15378538 [TBL] [Abstract][Full Text] [Related]
29. Dental characteristics of the Wolf-Hirschhorn syndrome: a case report. Babich SB; Banducci C; Teplitsky P Spec Care Dentist; 2004; 24(4):229-31. PubMed ID: 15462552 [TBL] [Abstract][Full Text] [Related]
32. Maxillary lateral incisor with two developmental grooves. Smith BE; Carroll B Oral Surg Oral Med Oral Pathol; 1990 Oct; 70(4):523-5. PubMed ID: 2216392 [No Abstract] [Full Text] [Related]
33. A Central Incisor with 4 Independent Root Canals: A Case Report. Aznar Portoles C; Moinzadeh AT; Shemesh H J Endod; 2015 Nov; 41(11):1903-6. PubMed ID: 26354384 [TBL] [Abstract][Full Text] [Related]
34. Taurodontism, shovel-shaped incisors and the Klinefelter syndrome. Gardner DG; Girgis SS Dent J; 1978 Sep; 44(8):372-3. PubMed ID: 278744 [No Abstract] [Full Text] [Related]
35. Clinical variability in KBG syndrome: report of three unrelated families. Maegawa GH; Leite JC; Félix TM; da Silveira HL; da Silveira HE Am J Med Genet A; 2004 Dec; 131(2):150-4. PubMed ID: 15384099 [TBL] [Abstract][Full Text] [Related]
36. Maxillary permanent incisors with two root canals: a report of two cases. Reid JS; Saunders WP; MacDonald DG Int Endod J; 1993 Jul; 26(4):246-50. PubMed ID: 8225644 [TBL] [Abstract][Full Text] [Related]
37. [Audiological phenotypes of KBG syndrome: a case report and literatures review]. Su W; Xia Y; Xia C; Liu Y Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2022 Oct; 36(10):797-801. PubMed ID: 36217662 [No Abstract] [Full Text] [Related]
38. Further delineation of the KBG syndrome phenotype caused by ANKRD11 aberrations. Ockeloen CW; Willemsen MH; de Munnik S; van Bon BW; de Leeuw N; Verrips A; Kant SG; Jones EA; Brunner HG; van Loon RL; Smeets EE; van Haelst MM; van Haaften G; Nordgren A; Malmgren H; Grigelioniene G; Vermeer S; Louro P; Ramos L; Maal TJ; van Heumen CC; Yntema HG; Carels CE; Kleefstra T Eur J Hum Genet; 2015 Sep; 23(9):1176-85. PubMed ID: 25424714 [TBL] [Abstract][Full Text] [Related]
39. Three root canals and dens formation in a maxillary lateral incisor: a case report. Walvekar SV; Behbehani JM J Endod; 1997 Mar; 23(3):185-6. PubMed ID: 9594762 [TBL] [Abstract][Full Text] [Related]
40. Haploinsufficiency for ANKRD11-flanking genes makes the difference between KBG and 16q24.3 microdeletion syndromes: 12 new cases. Novara F; Rinaldi B; Sisodiya SM; Coppola A; Giglio S; Stanzial F; Benedicenti F; Donaldson A; Andrieux J; Stapleton R; Weber A; Reho P; van Ravenswaaij-Arts C; Kerstjens-Frederikse WS; Vermeesch JR; Devriendt K; Bacino CA; Delahaye A; Maas SM; Iolascon A; Zuffardi O Eur J Hum Genet; 2017 Jun; 25(6):694-701. PubMed ID: 28422132 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]