140 related articles for article (PubMed ID: 15279406)
21. Short stature, microcephaly, characteristic face, syndactyly and mental retardation: the Filippi syndrome. Report on a second family.
Meinecke P
Genet Couns; 1993; 4(2):147-51. PubMed ID: 8395190
[TBL] [Abstract][Full Text] [Related]
22. A second patient with Tsukahara syndrome: type A1 brachydactyly, short stature, hearing loss, microcephaly, mental retardation and ptosis.
Utine GE; Breckpot J; Thienpont B; Alanay Y; Aksoy C; Boduroğlu K; Devriendt K
Am J Med Genet A; 2010 Apr; 152A(4):947-9. PubMed ID: 20358606
[TBL] [Abstract][Full Text] [Related]
23. Acrodysostosis. A syndrome of peripheral dysostosis, nasal hypoplasia, and mental retardation.
Robinow M; Pfeiffer RA; Gorlin RJ; McKusick VA; Renuart AW; Johnson GF; Summitt RL
Am J Dis Child; 1971 Mar; 121(3):195-203. PubMed ID: 5551869
[No Abstract] [Full Text] [Related]
24. Skeletal abnormalities in Rett syndrome: increasing evidence for dysmorphogenetic defects.
Leonard H; Thomson M; Bower C; Fyfe S; Constantinou J
Am J Med Genet; 1995 Sep; 58(3):282-5. PubMed ID: 8533832
[TBL] [Abstract][Full Text] [Related]
25. 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]
26. Triphalangeal thumb.
Qazi Q; Kassner EG
J Med Genet; 1988 Aug; 25(8):505-20. PubMed ID: 3050097
[TBL] [Abstract][Full Text] [Related]
27. Mental retardation with absent fifth fingernail and terminal phalanx.
Bartsocas CS; Tsiantos AK
Am J Dis Child; 1970 Nov; 120(5):493-4. PubMed ID: 5474762
[No Abstract] [Full Text] [Related]
28. [A case of congenital hypodactyly of the hand and foot].
Mamedov AG; Seidov MM
Ortop Travmatol Protez; 1991 Apr; (4):51-2. PubMed ID: 1754179
[No Abstract] [Full Text] [Related]
29. DOOR syndrome: clinical report, literature review and discussion of natural history.
James AW; Miranda SG; Culver K; Hall BD; Golabi M
Am J Med Genet A; 2007 Dec; 143A(23):2821-31. PubMed ID: 17994565
[TBL] [Abstract][Full Text] [Related]
30. DOOR syndrome: additional case and literature review.
Bos CJ; Ippel PF; Beemer FA
Clin Dysmorphol; 1994 Jan; 3(1):15-20. PubMed ID: 8205321
[TBL] [Abstract][Full Text] [Related]
31. Orthopaedic manifestations in de Barsy syndrome.
Stanton RP; Rao N; Scott CI
J Pediatr Orthop; 1994; 14(1):60-2. PubMed ID: 8113374
[TBL] [Abstract][Full Text] [Related]
32. [Idiopathic multicentric osteolysis with craniodysplasis and mental retardation: a new syndrome? (author's transl)].
Mathias K; Ludwig U
Rofo; 1977 Sep; 127(3):255-61. PubMed ID: 143430
[TBL] [Abstract][Full Text] [Related]
33. Acrodysostosis: autosomal dominant transmission.
Sheela SR; Perti A; Thomas G
Indian Pediatr; 2005 Aug; 42(8):822-6. PubMed ID: 16141486
[TBL] [Abstract][Full Text] [Related]
34. A syndrome with true anophthalmia, hand-foot defects and mental retardation.
Pallotta R; Dallapiccola B
Ophthalmic Paediatr Genet; 1984 Apr; 4(1):19-23. PubMed ID: 6544388
[TBL] [Abstract][Full Text] [Related]
35. Craniosynostosis with Marfan syndrome, hand and foot anomalies.
Shah AM; Chattopadhyay A; Kher A; Bharucha BA; Karapurkar AP
Clin Dysmorphol; 1996 Jul; 5(3):263-6. PubMed ID: 8818457
[TBL] [Abstract][Full Text] [Related]
36. Postaxial acrofacial dysostosis: report of a Brazilian patient.
Richieri-Costa A; Guion-Almeida ML
Am J Med Genet; 1989 Aug; 33(4):447-9. PubMed ID: 2596501
[TBL] [Abstract][Full Text] [Related]
37. 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]
38. Unusual type of brachydactyly associated with intraventricular septal defect and deafness: a new condition?
Camera G; Costa M
Clin Dysmorphol; 1997 Jan; 6(1):31-3. PubMed ID: 9018415
[TBL] [Abstract][Full Text] [Related]
39. F-syndrome (F-form of acro-pectoro-vertebral dysplasia): report on a second family.
Camera G; Camera A; Pozzolo S; Costa M; Mantero R
Am J Med Genet; 1995 Jul; 57(3):472-5. PubMed ID: 7677153
[TBL] [Abstract][Full Text] [Related]
40. Can Hutchinson-Gilford progeria syndrome be a neonatal condition?
Faivre L; Khau Van Kien P; Madinier-Chappat N; Nivelon-Chevallier A; Beer F; LeMerrer M
Am J Med Genet; 1999 Dec; 87(5):450-2; author reply 453-4. PubMed ID: 10594888
[No Abstract] [Full Text] [Related]
[Previous] [Next] [New Search]
