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3. 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]
4. The Coffin-Siris syndrome. Schinzel A Acta Paediatr Scand; 1979 May; 68(3):449-52. PubMed ID: 155976 [TBL] [Abstract][Full Text] [Related]
5. DOOR syndrome (deafness, onycho-osteodystrophy, and mental retardation): a new patient and delineation of neurologic variability among recessive cases. Lin HJ; Kakkis ED; Eteson DJ; Lachman RS Am J Med Genet; 1993 Sep; 47(4):534-9. PubMed ID: 8256819 [TBL] [Abstract][Full Text] [Related]
6. Deafness, onychodystrophy, osteodystrophy, mental retardation, and seizures (DOORS) syndrome: a new case report from Indonesia and review of the literature. Danarti R; Rahmayani S; Wirohadidjojo YW; Chen W Eur J Dermatol; 2020 Aug; 30(4):404-407. PubMed ID: 32969800 [TBL] [Abstract][Full Text] [Related]
7. A new case of DOOR syndrome. Wiśniewska M; Siwińska Z; Felczak M; Wielkoszyński T; Krawczyński M; Latos-Bieleńska A J Appl Genet; 2008; 49(1):101-3. PubMed ID: 18263975 [TBL] [Abstract][Full Text] [Related]
8. DOOR syndrome: report of three additional cases. Félix TM; de Menezes Karam S; Della Rosa VA; Moraes AM Clin Dysmorphol; 2002 Apr; 11(2):133-8. PubMed ID: 12002145 [TBL] [Abstract][Full Text] [Related]
9. Pre- and postnatal growth retardation--severe mental retardation--acral limb deficiencies with poorly keratinized nails. Another example of a distinct syndrome of inherited intrauterine dwarfism? Cartwright J; Nelson M; Fryns JP Genet Couns; 1991; 2(3):147-50. PubMed ID: 1801850 [TBL] [Abstract][Full Text] [Related]
10. [The Coffin-Siris syndrome. A new syndrome of mental retardation, hypo-aplasia of the nails and terminal phalanges of the 5th fingers and toes]. Mastroiacovo P; Salvaggio E; Parenti D Minerva Pediatr; 1977 Mar; 29(11):773-8. PubMed ID: 875947 [No Abstract] [Full Text] [Related]
11. Congenital heart disease and urinary tract abnormalities in two siblings with DOOR syndrome. Thornton CM; Magee AC; Thomas PS; Feakins R; Nevin NC; O'Hara MD Pediatr Pathol; 1994; 14(5):797-803. PubMed ID: 7808978 [TBL] [Abstract][Full Text] [Related]
12. [A dominant syndrome associated with polysyndactyly, spatule thumb, facial abnormalities, and mental retardation. (A particular form of Noack's acrocephalosyndactylia)]. Gnamey D; Farriaux JP J Genet Hum; 1971 Dec; 19(4):299-316. PubMed ID: 5152131 [No Abstract] [Full Text] [Related]
13. Familial absence of middle phalanges with nail dysplasia: a new syndrome. Bass HN Pediatrics; 1968 Aug; 42(2):318-23. PubMed ID: 5663738 [No Abstract] [Full Text] [Related]
14. Mental retardation with absent fifth fingernail and terminal phalanx. Coffin GS; Siris E Am J Dis Child; 1970 May; 119(5):433-9. PubMed ID: 5442442 [No Abstract] [Full Text] [Related]
15. 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]
16. 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]
17. DOORS syndrome: phenotype, genotype and comparison with Coffin-Siris syndrome. Campeau PM; Hennekam RC; Am J Med Genet C Semin Med Genet; 2014 Sep; 166C(3):327-32. PubMed ID: 25169651 [TBL] [Abstract][Full Text] [Related]
18. 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]
19. A new multiple congenital anomaly, mental retardation syndrome with preaxial brachydactyly, hyperphalangism, deafness and orodental anomalies. Temtamy SA; Meguid NA; Ismail SI; Ramzy MI Clin Dysmorphol; 1998 Oct; 7(4):249-55. PubMed ID: 9823490 [TBL] [Abstract][Full Text] [Related]
20. Pure 9p duplication syndrome with aplasia of the middle phalanges of the fifth fingers. Sato A; Suzuki T; Ikeno M; Takeda J; Yamamoto Y; Shinohara M; Makino S; Takeda S; Shimizu T; Itakura A Eur J Med Genet; 2020 Oct; 63(10):104005. PubMed ID: 32693209 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]