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3. Report of four familial cases with congenitally missing mandibular incisors. Newman GV; Newman RA Am J Orthod Dentofacial Orthop; 1998 Aug; 114(2):195-207. PubMed ID: 9714285 [TBL] [Abstract][Full Text] [Related]
4. [Simultaneous occurence of hyperdontia and hypodontia]. Novák J Sb Ved Pr Lek Fak Karlovy Univerzity Hradci Kralove Suppl; 1974; 17(5):467-71. PubMed ID: 4534820 [No Abstract] [Full Text] [Related]
5. Genetics--a tool for the dentist. Report of a case of inherited oligodontia. Gertzman GB Clin Prev Dent; 1982; 4(1):19-21. PubMed ID: 6980080 [No Abstract] [Full Text] [Related]
6. [Oligodontia as an orthodontic problem]. Adler-Hradecky C; Adler P Osterr Z Stomatol; 1969 Aug; 66(8):294-7. PubMed ID: 5260215 [No Abstract] [Full Text] [Related]
7. The orthodontic-restorative interface in the younger patient. J Ir Dent Assoc; 1995; 41(3):46-55. PubMed ID: 8975066 [No Abstract] [Full Text] [Related]
8. Oral rehabilitation of a patient with congenital partial anodontia using a rotational path removable partial denture: report of a case. Reagan SE; Dao TM Quintessence Int; 1995 Mar; 26(3):181-5. PubMed ID: 7568733 [TBL] [Abstract][Full Text] [Related]
10. Hypodontia with nail dysgenesis. Santavá A; Nováková K; Santavý J Acta Univ Palacki Olomuc Fac Med; 1983; 104():333-41. PubMed ID: 6222618 [No Abstract] [Full Text] [Related]
11. Genealogy and consequences of congenitally missing second premolars. Svedmyr B J Int Assoc Dent Child; 1983 Dec; 14(2):77-82. PubMed ID: 6586858 [No Abstract] [Full Text] [Related]
12. [Oligodontia or partial anodontia (report of 3 cases)]. Thasanabanchong S J Dent Assoc Thai; 1981; 31(2):63-74. PubMed ID: 6946104 [No Abstract] [Full Text] [Related]
13. [Individualization and evaluation of tooth agenesis in relation to orthodontic problems]. Tollaro I; Vichi M Mondo Ortod; 1982; 7(2):31-41. PubMed ID: 6962365 [No Abstract] [Full Text] [Related]
14. Oligodontia: report of a family. Ruprecht A; Sastry KA; Batniji S; Mohammad AR; Al-Saleh H Ann Dent; 1985; 44(1):35-8. PubMed ID: 3863539 [No Abstract] [Full Text] [Related]
15. MSX1 mutation is associated with orofacial clefting and tooth agenesis in humans. van den Boogaard MJ; Dorland M; Beemer FA; van Amstel HK Nat Genet; 2000 Apr; 24(4):342-3. PubMed ID: 10742093 [No Abstract] [Full Text] [Related]
16. [Movement of opposing position of each tooth for malocclusion case (author's transl)]. Komuro H Shikwa Gakuho; 1975 Nov; 75(11):1564-8. PubMed ID: 1074271 [No Abstract] [Full Text] [Related]
17. Rieger's syndrome. Severe dental anomalies with mild ophthalmic changes--a case report. Lapeer GL J Can Dent Assoc; 1986 Nov; 52(11):935-7. PubMed ID: 3539283 [No Abstract] [Full Text] [Related]
18. [Case of familial hypodontia]. Re G; Re S; Chicco R Minerva Stomatol; 1980; 29(3):209-17. PubMed ID: 6935512 [TBL] [Abstract][Full Text] [Related]
19. [Orthodontic treatment of malocclusion with mandibular congenital missing teeth guided by Bolton index]. Duan YZ; Sun YM; Zhang YF; Jin F; Leng J Zhonghua Kou Qiang Yi Xue Za Zhi; 2003 Jan; 38(1):43-5. PubMed ID: 12760776 [TBL] [Abstract][Full Text] [Related]
20. [A case of familial partial agenesis]. Lo Muzio L; Mignogna MD; Zunino AF Stomatol Mediterr; 1986; 6(4):545-51. PubMed ID: 3474794 [No Abstract] [Full Text] [Related] [Next] [New Search]