These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
106 related articles for article (PubMed ID: 10631927)
21. [Gene mapping on Blepharophimosis Epicanthus Inversus and Ptosis syndrome type I in Chinese family]. Zhang W; Pang H; Shi H; Huang S Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2001 Feb; 18(1):8-10. PubMed ID: 11172632 [TBL] [Abstract][Full Text] [Related]
22. Marden-Walker phenotype: spectrum of variability in three infants. Ramer JC; Frankel CA; Ladda RL Am J Med Genet; 1993 Feb; 45(3):285-91. PubMed ID: 7679543 [TBL] [Abstract][Full Text] [Related]
23. [Hereditary blepharophimosis with visual alterations]. Ruíz-Manjarrez A; Guillén-Añorve B; Núñez-Gómez R Bol Med Hosp Infant Mex; 1993 Aug; 50(8):586-9. PubMed ID: 8357520 [TBL] [Abstract][Full Text] [Related]
24. [Marden-Walker syndrome--a case report]. Dumić M; Rojnić-Putarek N; Skrablin-Kucić S; Matić T; Ille J; Radica A Lijec Vjesn; 2009; 131(7-8):203-6. PubMed ID: 19769282 [TBL] [Abstract][Full Text] [Related]
25. Mutations in MED12 cause X-linked Ohdo syndrome. Vulto-van Silfhout AT; de Vries BB; van Bon BW; Hoischen A; Ruiterkamp-Versteeg M; Gilissen C; Gao F; van Zwam M; Harteveld CL; van Essen AJ; Hamel BC; Kleefstra T; Willemsen MA; Yntema HG; van Bokhoven H; Brunner HG; Boyer TG; de Brouwer AP Am J Hum Genet; 2013 Mar; 92(3):401-6. PubMed ID: 23395478 [TBL] [Abstract][Full Text] [Related]
26. Unknown syndrome in two male sibs with hypotonia, ptosis, hand malformations, 2/3 toes syndactyly, and mental retardation. Mégarbané A; Farah CB; Nabbout R Genet Couns; 1999; 10(2):183-8. PubMed ID: 10422013 [TBL] [Abstract][Full Text] [Related]
30. [Blepharophimosis, ptosis and epicanthus inversus syndrome plus sensorineural deafness]. Pérez-Caballero Macarrón C; Quintana Castilla A; Aparicio Meix JM An Esp Pediatr; 1999 Nov; 51(5):530-2. PubMed ID: 10652806 [No Abstract] [Full Text] [Related]
31. A clinical and genetic study of the Say/Barber/Biesecker/Young-Simpson type of Ohdo syndrome. Day R; Beckett B; Donnai D; Fryer A; Heidenblad M; Howard P; Kerr B; Mansour S; Maye U; McKee S; Mohammed S; Sweeney E; Tassabehji M; de Vries BB; Clayton-Smith J Clin Genet; 2008 Nov; 74(5):434-44. PubMed ID: 18798845 [TBL] [Abstract][Full Text] [Related]
32. Deletion 2q37: an identifiable clinical syndrome with mental retardation and autism. Galasso C; Lo-Castro A; Lalli C; Nardone AM; Gullotta F; Curatolo P J Child Neurol; 2008 Jul; 23(7):802-6. PubMed ID: 18658079 [TBL] [Abstract][Full Text] [Related]
33. Mental retardation, obesity, mandibular prognathism with eye and skin anomalies (MOMES syndrome): a newly recognized autosomal recessive syndrome. Kantaputra PN; Kunachaichote J; Patikulsila P Am J Med Genet; 2001 Nov; 103(4):283-8. PubMed ID: 11746007 [TBL] [Abstract][Full Text] [Related]
34. Van der Woude syndrome with mental retardation: case report. Ugwu BT; Momoh JT East Afr Med J; 2001 Feb; 78(2):111-2. PubMed ID: 11682943 [TBL] [Abstract][Full Text] [Related]
35. [Congenital blepharophimosis, ptosis and epicanthus inversus in a Balinese (Indonesia) family]. Ney R; Breguet G Rev Med Suisse Romande; 1981 Apr; 101(4):269-72. PubMed ID: 7256058 [No Abstract] [Full Text] [Related]
37. The KBG syndrome: an additional sporadic case. Mathieu M; Helou M; Morin G; Dolhem P; Devauchelle B; Piussan C Genet Couns; 2000; 11(1):33-5. PubMed ID: 10756425 [TBL] [Abstract][Full Text] [Related]
38. Newly recognized blepharofacioskeletal syndrome. Richieri-Costa A; Guion-Almeida ML; Rodini ES; Pereira SC; Cohen MM Am J Med Genet; 1993 Jul; 46(6):620-2. PubMed ID: 8362901 [TBL] [Abstract][Full Text] [Related]
39. Blepharophimosis, eczema, and growth and developmental delay in a young adult: late features of Dubowitz syndrome? Lyonnet S; Schwartz G; Gatin G; de Prost Y; Munnich A; Le Merrer M J Med Genet; 1992 Jan; 29(1):68-9. PubMed ID: 1552551 [TBL] [Abstract][Full Text] [Related]
40. Two further cases of Ohdo syndrome delineate the phenotypic variability of the condition. White SM; Adès LC; Amor D; Liebelt J; Bankier A; Baker E; Wilson M; Savarirayan R Clin Dysmorphol; 2003 Apr; 12(2):109-13. PubMed ID: 12868473 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]