110 related articles for article (PubMed ID: 3481527)
21. Identification of a mutation in DLX3 associated with tricho-dento-osseous (TDO) syndrome.
Price JA; Bowden DW; Wright JT; Pettenati MJ; Hart TC
Hum Mol Genet; 1998 Mar; 7(3):563-9. PubMed ID: 9467018
[TBL] [Abstract][Full Text] [Related]
22. Clinical heterogeneity in the tricho-dento-osseous syndrome.
Quattromani F; Shapiro SD; Young RS; Jorgenson RJ; Parker JW; Blumhardt R; Reece RR
Hum Genet; 1983; 64(2):116-21. PubMed ID: 6885044
[TBL] [Abstract][Full Text] [Related]
23. Craniofacial morphology of the tricho-dento-osseous syndrome.
Kula K; Hall K; Hart T; Wright JT
Clin Genet; 1996 Dec; 50(6):446-54. PubMed ID: 9147871
[TBL] [Abstract][Full Text] [Related]
24. Oral and craniofacial morphology of a patient with Larsen syndrome.
Tsang MC; Ling JY; King NM; Chow SK
J Craniofac Genet Dev Biol; 1986; 6(4):357-62. PubMed ID: 3793859
[TBL] [Abstract][Full Text] [Related]
25. [Facial hemihyperplasia associated with strabismus inherited by dominant trait].
Bencze J; Schnitzler A; Walawska J
Orv Hetil; 1972 Sep; 113(36):2172-5. PubMed ID: 5051104
[No Abstract] [Full Text] [Related]
26. [Tricho-odonto-onycho-syndrome in hyphydrotic form based on two cases].
Csiba A; Dénes Z; Szakály T
Fogorv Sz; 1998 Jan; 91(1):13-7. PubMed ID: 9465470
[TBL] [Abstract][Full Text] [Related]
27. Characterization and mRNA expression in an unusual odontogenic lesion in a patient with tricho-dento-osseous syndrome.
Dodds AP; Cox SA; Suggs CA; Boyd C; Ruiz R; Hart TC; Wright JT
Histol Histopathol; 2003 Jul; 18(3):849-54. PubMed ID: 12792897
[TBL] [Abstract][Full Text] [Related]
28. A novel GJA 1 mutation in oculo-dento-digital dysplasia with curly hair and hyperkeratosis.
Kelly SC; Ratajczak P; Keller M; Purcell SM; Griffin T; Richard G
Eur J Dermatol; 2006; 16(3):241-5. PubMed ID: 16709485
[TBL] [Abstract][Full Text] [Related]
29. Syndrome of dental anomalies, curly hair and sclerotic bones.
Lichtenstein JR; Warson RW
Birth Defects Orig Artic Ser; 1971 Jun; 7(7):308-11. PubMed ID: 5173238
[No Abstract] [Full Text] [Related]
30. Facial and oral findings in trichorhinophalangeal syndrome type 1 (characteristics of TRPS 1).
Bennett CG; Hill CJ; Frias JL
Pediatr Dent; 1981 Dec; 3(4):348-52. PubMed ID: 6952172
[No Abstract] [Full Text] [Related]
31. Morphological appearance and chemical composition of enamel in primary teeth from patients with 22q11 deletion syndrome.
Klingberg G; Dietz W; Oskarsdóttir S; Odelius H; Gelander L; Norén JG
Eur J Oral Sci; 2005 Aug; 113(4):303-11. PubMed ID: 16048522
[TBL] [Abstract][Full Text] [Related]
32. A common DLX3 gene mutation is responsible for tricho-dento-osseous syndrome in Virginia and North Carolina families.
Price JA; Wright JT; Kula K; Bowden DW; Hart TC
J Med Genet; 1998 Oct; 35(10):825-8. PubMed ID: 9783705
[TBL] [Abstract][Full Text] [Related]
33. [Incidence, pathological significance and genetic problems of a central enamel ridge in human premolars].
Zuhrt R; Solyga P
Dtsch Stomatol; 1967 Oct; 17(10):770-8. PubMed ID: 5235197
[No Abstract] [Full Text] [Related]
34. [Basocellular nevomatosis: a syndrome of stomatological importance. Notes on 3 clinical cases].
Fiamminghi L; Gazzotti A; Bonanini M; Bozzetti A
Minerva Stomatol; 1982; 31(4):443-8. PubMed ID: 6958962
[No Abstract] [Full Text] [Related]
35. [Pilo-dento-ungular dysplasia with microcephaly].
Narahara K
Ryoikibetsu Shokogun Shirizu; 2001; (34 Pt 2):505-6. PubMed ID: 11528864
[No Abstract] [Full Text] [Related]
36. Lacrimo-auriculo-dento-digital syndrome: a literature review and case reports.
Toumba KJ; Gutteridge DL
Quintessence Int; 1995 Dec; 26(12):829-39. PubMed ID: 8596813
[TBL] [Abstract][Full Text] [Related]
37. Orodental findings and genetic disorders.
Salinas CF
Birth Defects Orig Artic Ser; 1982; 18(1):79-120. PubMed ID: 7115915
[No Abstract] [Full Text] [Related]
38. [Oculo-mandibulo-facial syndrome].
Stolovitch H; Bracha R; Godel V
Harefuah; 1984 Dec; 107(11):330-2. PubMed ID: 6442256
[No Abstract] [Full Text] [Related]
39. Craniofacial anomalies, abnormal hair, camptodactyly, and caudal appendage (Teebi-Shaltout syndrome): clinical and autopsy findings.
Froster UG; Rehder H; Höhn W; Oberheuser F
Am J Med Genet; 1993 Oct; 47(5):717-22. PubMed ID: 8267003
[TBL] [Abstract][Full Text] [Related]
40. Dental and craniofacial features of Aarskog syndrome: report of a case and review of literature.
Reddy P; Kharbanda OP; Kabra M; Duggal R
J Clin Pediatr Dent; 1999; 23(2):155-9. PubMed ID: 10204459
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
