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7. Hereditary gingival fibromatosis and sensorineural hearing loss in a 42-year-old man with Jones syndrome. Kasaboğlu O; Tümer C; Balci S Genet Couns; 2004; 15(2):213-8. PubMed ID: 15287422 [TBL] [Abstract][Full Text] [Related]
8. The phenotypic overlap of syndromes associated with hereditary gingival fibromatosis: follow-up of a family for five years. Haytac MC; Ozcelik O Oral Surg Oral Med Oral Pathol Oral Radiol Endod; 2007 Apr; 103(4):521-7. PubMed ID: 17395066 [TBL] [Abstract][Full Text] [Related]
9. [Pediatric dentistry syndrome with various oro-systemic congenital abnormalities (condroectodermal dysplasia or oro-digital-facial disorders); presentation of a case]. Menendez OR; Perez ER Cent Estud Recur Odontol Nino; 1981 Apr; 6(1):45-50. PubMed ID: 6942943 [No Abstract] [Full Text] [Related]
10. Hereditary gingival fibromatosis with distinct dental, skeletal and developmental abnormalities. Katz J; Guelmann M; Barak S Pediatr Dent; 2002; 24(3):253-6. PubMed ID: 12064501 [TBL] [Abstract][Full Text] [Related]
11. Zimmermann-Laband syndrome with bilateral developmental cataract - a new association? Shah N; Gupta YK; Ghose S Int J Paediatr Dent; 2004 Jan; 14(1):78-85. PubMed ID: 14706033 [TBL] [Abstract][Full Text] [Related]
12. Congenital malformation: dental features of acardia--case report. Dean D; Ceballos R J Oral Med; 1985; 40(3):106-7. PubMed ID: 3861808 [No Abstract] [Full Text] [Related]
13. Laband syndrome. Report of two cases, review of the literature, and identification of additional manifestations. Chadwick B; Hunter B; Hunter L; Aldred M; Wilkie A Oral Surg Oral Med Oral Pathol; 1994 Jul; 78(1):57-63. PubMed ID: 8078665 [TBL] [Abstract][Full Text] [Related]
14. Zimmermann-Laband syndrome in a patient with severe mental retardation. Van Buggenhout GJ; Brunner HG; Trommelen JC; Hamel BC Genet Couns; 1995; 6(4):321-7. PubMed ID: 8775419 [TBL] [Abstract][Full Text] [Related]
15. Hereditary gingival fibromatosis associated with hearing loss and supernumerary teeth--a new syndrome. Wynne SE; Aldred MJ; Bartold PM J Periodontol; 1995 Jan; 66(1):75-9. PubMed ID: 7891255 [TBL] [Abstract][Full Text] [Related]
16. Syndrome identification case report 89: thickened subcutaneous tissue, coarse facies, macrocephaly, and hypotonia. Hillig U J Clin Dysmorphol; 1983; 1(1):9-12. PubMed ID: 6580387 [No Abstract] [Full Text] [Related]
17. Bartsocas-Papas syndrome. A case report. Cheirif S; Grayson BH; Maccaro HA N Y State Dent J; 1985 Feb; 51(2):101-2. PubMed ID: 2984611 [No Abstract] [Full Text] [Related]
18. Gingival fibromatosis and growth hormone deficiency syndrome--report of a rare case and review of literature. Radhakrishnan S; Rajan P Indian J Dent Res; 2003; 14(3):170-2. PubMed ID: 15164660 [TBL] [Abstract][Full Text] [Related]
19. Syndrome identification case report 90: multiple craniofacial and skeletal defects. Mastroiacovo P; De Rosa G; Satta MA; Colavita N; Priolo F; Pasargiklian E J Clin Dysmorphol; 1983; 1(1):13-5. PubMed ID: 6580383 [No Abstract] [Full Text] [Related]
20. Zimmermann-Laband syndrome: a case report. Sawaki K; Mishima K; Sato A; Goda Y; Osugi A; Nakano M J Clin Pediatr Dent; 2012; 36(3):297-300. PubMed ID: 22838235 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]