131 related articles for article (PubMed ID: 5516283)
1. [Familial deafness with osteo-onycho-dysplasia].
Walbaum R; Fontaine G; Lienhardt J; Piquet JJ
J Genet Hum; 1970 May; 18(1):101-8. PubMed ID: 5516283
[No Abstract] [Full Text] [Related]
2. Deafness, onycho-osteodystrophy, mental retardation (DOOR) syndrome.
Nevin NC; Thomas PS; Calvert J; Reid MM
Am J Med Genet; 1982 Nov; 13(3):325-32. PubMed ID: 7180877
[No Abstract] [Full Text] [Related]
3. [Familial craniometaphyseal dysplasia associated with mental retardation].
Portnov VA; Marincheva GS; Gorbachevskaia NL
Zh Nevropatol Psikhiatr Im S S Korsakova; 1985; 85(3):404-9. PubMed ID: 3993302
[TBL] [Abstract][Full Text] [Related]
4. Congenital sensori-neural deafness associated with onycho-osteo dystrophy and mental retardation (D.O.O.R. syndrome).
Cantwell RJ
Humangenetik; 1975; 26(3):261-5. PubMed ID: 1132883
[TBL] [Abstract][Full Text] [Related]
5. [Polydysplasia with dermal hypoplasia in some areas].
Stewart WM; Lauret P; Michel Y
Bull Soc Fr Dermatol Syphiligr; 1969; 76(6):812-4. PubMed ID: 5396013
[No Abstract] [Full Text] [Related]
6. A bone dysplasia with deafness.
Insley J; Astley R
Br J Radiol; 1974 May; 47(557):244-51. PubMed ID: 4830146
[No Abstract] [Full Text] [Related]
7. [Osteo-onycho dysplasia--a rare hereditary malformation].
Fankhaenel R
Beitr Orthop Traumatol; 1972 Apr; 19(4):236-9. PubMed ID: 5051296
[No Abstract] [Full Text] [Related]
8. [Case of fibrous dysplasia of the bones of the face and the skull associated with mental retardation with epilepsy and unilateral deafness].
Wintgens M; Roland T; Evrard M
Acta Paediatr Belg; 1968; 22(1):29-40. PubMed ID: 5759451
[No Abstract] [Full Text] [Related]
9. Hereditary sensorineural hearing loss associated with onychodystrophy and digital malformations.
Moghadam H; Statten P
Can Med Assoc J; 1972 Aug; 107(4):310-2. PubMed ID: 5056117
[No Abstract] [Full Text] [Related]
10. Additional case report of the DOOR syndrome.
Hess RO; Pecotte JK
Am J Med Genet; 1984 Oct; 19(2):401-5. PubMed ID: 6507487
[No Abstract] [Full Text] [Related]
11. DOOR syndrome (deafness, onycho-osteodystrophy, and mental retardation): elevated plasma and urinary 2-oxoglutarate in three unrelated patients.
Patton MA; Krywawych S; Winter RM; Brenton DP; Baraitser M
Am J Med Genet; 1987 Jan; 26(1):207-15. PubMed ID: 3812564
[TBL] [Abstract][Full Text] [Related]
12. [Deafness-onycho-osteodystrophy-retardation-seizures (DOORS)].
Kosuga M; Okuyama T
Ryoikibetsu Shokogun Shirizu; 2001; (33):537-8. PubMed ID: 11462556
[No Abstract] [Full Text] [Related]
13. [Onychodystrophy associated with perceptive deafness].
Berbescu C; Bogdan C; Christodorescu D; Pascu A
Rev Chir Oncol Radiol O R L Oftalmol Stomatol Otorinolaringol; 1982; 27(2):131-5. PubMed ID: 6216525
[No Abstract] [Full Text] [Related]
14. Skeletal dysplasias and mental retardation.
Chen H
Prog Clin Biol Res; 1982; 104():451-85. PubMed ID: 6761697
[No Abstract] [Full Text] [Related]
15. Skeletal dysplasia, hyperpigmentation, cutis laxa, endocrine abnormality, and mental retardation--the Patterson syndrome.
David TJ
Prog Clin Biol Res; 1982; 104():331-7. PubMed ID: 7163277
[No Abstract] [Full Text] [Related]
16. [Iso-Kikuchi syndrome. Congenital onychodysplasia].
Brunzlow H; Loreck D; Neumann J
Radiol Diagn (Berl); 1987; 28(6):773-81. PubMed ID: 3448622
[No Abstract] [Full Text] [Related]
17. Coats' disease and muscular dystrophy.
Small RG
Trans Am Acad Ophthalmol Otolaryngol; 1968; 72(2):225-31. PubMed ID: 5659903
[No Abstract] [Full Text] [Related]
18. Dystrophia retinae pigmentosa--dysacusis syndrome (DRD): a study of the Usher- or Hallgren syndrome.
Nuutila A
J Genet Hum; 1970 May; 18(1):57-88. PubMed ID: 5516287
[No Abstract] [Full Text] [Related]
19. Tooth root resorption associated with a familial bone dysplasia affecting mother and daughter.
Olsen CB; Tangchaitrong K; Chippendale I; Graham HK; Dahl HM; Stockigt JR
Pediatr Dent; 1999; 21(6):363-7. PubMed ID: 10509339
[TBL] [Abstract][Full Text] [Related]
20. Fountain syndrome: further delineation of the clinical syndrome and follow-up data.
Van Buggenhout GJ; Van Ravenswaaij-Arts CM; Renier WO; Van de Wiel MP; Trommelen JC; Pijkels E; Hamel BC; Fryns JP
Genet Couns; 1996; 7(3):177-86. PubMed ID: 8897038
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
