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.
2. Polydactyly, conical teeth, nail dysplasia, and short limbs: a new autosomal dominant malformation syndrome. Curry CJ; Hall BD Birth Defects Orig Artic Ser; 1979; 15(5B):253-63. PubMed ID: 526581 [No Abstract] [Full Text] [Related]
3. ADULT-syndrome: an autosomal-dominant disorder with pigment anomalies, ectrodactyly, nail dysplasia, and hypodontia. Propping P; Zerres K Am J Med Genet; 1993 Mar; 45(5):642-8. PubMed ID: 8456838 [TBL] [Abstract][Full Text] [Related]
4. A new syndrome of dwarfism, brachydactyly, nail dysplasia, and mental retardation in sibs. Tonoki H; Kishino T; Niikawa N Am J Med Genet; 1990 May; 36(1):89-93. PubMed ID: 2333912 [TBL] [Abstract][Full Text] [Related]
5. Tricho-dento-osseous syndrome: heterogeneity or clinical variability. Shapiro SD; Quattromani FL; Jorgenson RJ; Young RS Am J Med Genet; 1983 Oct; 16(2):225-36. PubMed ID: 6650567 [TBL] [Abstract][Full Text] [Related]
6. 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]
7. Hereditary hypodontia and onychorrhexis of the fingernails and toenail koilonychia: Witkop's tooth-and nail syndrome. Zabawski EJ; Cohen JB Dermatol Online J; 1999 May; 5(1):3. PubMed ID: 10673446 [TBL] [Abstract][Full Text] [Related]
9. Syndrome of polydactyly, conical teeth and nail dysplasia. Roubicek M; Spranger J Am J Med Genet; 1985 Jan; 20(1):205-7. PubMed ID: 2982263 [No Abstract] [Full Text] [Related]
10. Report of a new syndrome: focus on differential diagnosis and review of Ellis-van Creveld, Curry-Hall, acrofacial dysostosis, and orofacial digital syndromes. Ghosh S; Setty S; Sivakumar A; Pai KM Oral Surg Oral Med Oral Pathol Oral Radiol Endod; 2007 May; 103(5):670-6. PubMed ID: 17466885 [TBL] [Abstract][Full Text] [Related]
11. Acro-renal-ocular syndrome: autosomal dominant thumb hypoplasia, renal ectopia, and eye defect. Halal F; Homsy M; Perreault G Am J Med Genet; 1984 Apr; 17(4):753-62. PubMed ID: 6426304 [TBL] [Abstract][Full Text] [Related]
18. A rare case of tooth-nail syndrome. Mielnik-Błaszczak M; Tomankiewicz M Ann Univ Mariae Curie Sklodowska Med; 2003; 58(2):306-10. PubMed ID: 15323210 [TBL] [Abstract][Full Text] [Related]
19. Keratin 17 mutation in pachyonychia congenita type 2 patient with early onset steatocystoma multiplex and Hutchinson-like tooth deformity. Oh SW; Kim MY; Lee JS; Kim SC J Dermatol; 2006 Mar; 33(3):161-4. PubMed ID: 16620218 [TBL] [Abstract][Full Text] [Related]
20. Polydactyly: report of a large kindred. Kirkland LR; Russell RO South Med J; 1976 Apr; 69(4):436-7. PubMed ID: 1265503 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]