153 related articles for article (PubMed ID: 8696323)
1. Two genes for missing teeth.
Thesleff I
Nat Genet; 1996 Aug; 13(4):379-80. PubMed ID: 8696323
[No Abstract] [Full Text] [Related]
2. A human MSX1 homeodomain missense mutation causes selective tooth agenesis.
Vastardis H; Karimbux N; Guthua SW; Seidman JG; Seidman CE
Nat Genet; 1996 Aug; 13(4):417-21. PubMed ID: 8696335
[TBL] [Abstract][Full Text] [Related]
3. Role of genes in oro-dental diseases.
Kavitha B; Priyadharshini V; Sivapathasundharam B; Saraswathi TR
Indian J Dent Res; 2010; 21(2):270-4. PubMed ID: 20657100
[TBL] [Abstract][Full Text] [Related]
4. A genetic study of anodontia in X-linked hypohidrotic ectodermal dysplasia.
Nakata M; Koshiba H; Eto K; Nance WE
Am J Hum Genet; 1980 Nov; 32(6):908-19. PubMed ID: 7446529
[TBL] [Abstract][Full Text] [Related]
5. Craniofacial disorders caused by mutations in homeobox genes MSX1 and MSX2.
Cohen MM
J Craniofac Genet Dev Biol; 2000; 20(1):19-25. PubMed ID: 10879654
[TBL] [Abstract][Full Text] [Related]
6. A family history of hereditary anhidrotic mesodermal-ectodermal dysplasia.
Cook WA; Kane FJ
J Am Dent Assoc; 1968 May; 76(5):1032-7. PubMed ID: 5239025
[No Abstract] [Full Text] [Related]
7. Gene defect in hypodontia: exclusion of MSX1 and MSX2 as candidate genes.
Nieminen P; Arte S; Pirinen S; Peltonen L; Thesleff I
Hum Genet; 1995 Sep; 96(3):305-8. PubMed ID: 7649547
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Absence of mutations in the homeodomain of the MSX1 gene in patients with hypodontia.
Scarel RM; Trevilatto PC; Di Hipólito O; Camargo LE; Line SR
Am J Med Genet; 2000 Jun; 92(5):346-9. PubMed ID: 10861665
[TBL] [Abstract][Full Text] [Related]
10. Molecular morphogenetic fields in the development of human dentition.
Line SR
J Theor Biol; 2001 Jul; 211(1):67-75. PubMed ID: 11407892
[TBL] [Abstract][Full Text] [Related]
11. Common genetic defects of the mouth.
Sanger RG
Dent Assist (1931); 1975 Jun; 44(6):20-6. PubMed ID: 1074365
[No Abstract] [Full Text] [Related]
12. The genetic basis of inherited anomalies of the teeth. Part 2: syndromes with significant dental involvement.
Bailleul-Forestier I; Berdal A; Vinckier F; de Ravel T; Fryns JP; Verloes A
Eur J Med Genet; 2008; 51(5):383-408. PubMed ID: 18599376
[TBL] [Abstract][Full Text] [Related]
13. [Missing teeth abnormalities in ectodermic dysplasias].
Marenduzzo A
Arch Stomatol (Napoli); 1968; 9(3):245-55. PubMed ID: 5274019
[No Abstract] [Full Text] [Related]
14. The role of MSX1 in human tooth agenesis.
Lidral AC; Reising BC
J Dent Res; 2002 Apr; 81(4):274-8. PubMed ID: 12097313
[TBL] [Abstract][Full Text] [Related]
15. Congenital absence of teeth: a review with emphasis on inheritance patterns.
Graber LW
J Am Dent Assoc; 1978 Feb; 96(2):266-75. PubMed ID: 342579
[TBL] [Abstract][Full Text] [Related]
16. [Basan's syndrome: dominant autosomal hypohidrotic ectodermal dysplasia].
Hernando I; Benavides A; Plasencia A; Visus EP; Bousoño C; Fernández Toral J
An Esp Pediatr; 1988 Apr; 28(4):359-60. PubMed ID: 3400948
[No Abstract] [Full Text] [Related]
17. ADULT ectodermal dysplasia syndrome resulting from the missense mutation R298Q in the p63 gene.
Chan I; Harper JI; Mellerio JE; McGrath JA
Clin Exp Dermatol; 2004 Nov; 29(6):669-72. PubMed ID: 15550149
[TBL] [Abstract][Full Text] [Related]
18. [Anhidrotic ectodermal dysplasia associated with anodontia and its genetic pattern].
Nakata M; Koshiba Y
Kokubyo Gakkai Zasshi; 1976 Jun; 43(2):185-6. PubMed ID: 1069057
[No Abstract] [Full Text] [Related]
19. Hereditary ectodermal dysplasia: report of a case.
Alexander WN; Cahill RJ
ASDC J Dent Child; 1969; 36(4):265 passim. PubMed ID: 4893602
[No Abstract] [Full Text] [Related]
20. [Anodontic anhydrotic ectodermal dysplasia].
Jourdain JC; Lelorier B; Larrègue M
Ann Dermatol Venereol; 1984; 111(10):939-40. PubMed ID: 6524811
[No Abstract] [Full Text] [Related]
[Next] [New Search]