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.
137 related articles for article (PubMed ID: 20523806)
21. A family with branchio-oculo-facial syndrome with primarily ocular involvement associated with mutation of the TFAP2A gene. Dumitrescu AV; Milunsky JM; Longmuir SQ; Drack AV Ophthalmic Genet; 2012 Jun; 33(2):100-6. PubMed ID: 22191992 [TBL] [Abstract][Full Text] [Related]
22. [New oral manifestations of Branchio-oculo-facial syndrome. Case report]. García Flores JB; Escamilla Ocañas CE; Martínez Menchaca HR; Treviño Alanís MG; Rivera Silva G Arch Argent Pediatr; 2015 Jan; 113(1):e14-6. PubMed ID: 25622170 [TBL] [Abstract][Full Text] [Related]
23. Branchio-oculo-facial syndrome (BOFS) and congenital heart defects. Rosa RF; Zen PR; Graziadio C; Paskulin GA Arq Bras Cardiol; 2009 Feb; 92(2):e6-8, e33-5. PubMed ID: 19360235 [TBL] [Abstract][Full Text] [Related]
24. New autosomal dominant branchio-oculo-facial syndrome. Fujimoto A; Lipson M; Lacro RV; Shinno NW; Boelter WD; Jones KL; Wilson MG Am J Med Genet; 1987 Aug; 27(4):943-51. PubMed ID: 3321995 [TBL] [Abstract][Full Text] [Related]
25. Branchio-oculo-facial syndrome with bilateral linear scars of the neck. El Darouti MA; Marzouk SA; Azzam OA; Nada HR; Sobhi RM; El Nabarawi I Int J Dermatol; 2005 Aug; 44(8):674-6. PubMed ID: 16101871 [TBL] [Abstract][Full Text] [Related]
27. Treatment of otorhinolaryngological manifestations of three rare genetic syndromes: Branchio-Oculo-Facial (BOF), Ectrodactyly Ectodermal dysplasia Clefting (EEC) and focal dermal hypoplasia (Goltz syndrome). Skarzynski H; Podskarbi-Fayette R Int J Pediatr Otorhinolaryngol; 2009 Jan; 73(1):143-51. PubMed ID: 19012972 [TBL] [Abstract][Full Text] [Related]
28. Genotype-phenotype analysis of the branchio-oculo-facial syndrome. Milunsky JM; Maher TM; Zhao G; Wang Z; Mulliken JB; Chitayat D; Clemens M; Stalker HJ; Bauer M; Burch M; Chénier S; Cunningham ML; Drack AV; Janssens S; Karlea A; Klatt R; Kini U; Klein O; Lachmeijer AM; Megarbane A; Mendelsohn NJ; Meschino WS; Mortier GR; Parkash S; Ray CR; Roberts A; Roberts A; Reardon W; Schnur RE; Smith R; Splitt M; Tezcan K; Whiteford ML; Wong DA; Zori R; Lin AE Am J Med Genet A; 2011 Jan; 155A(1):22-32. PubMed ID: 21204207 [TBL] [Abstract][Full Text] [Related]
32. Thymic tissue in the skin: a clue to the diagnosis of the branchio-oculo-facial syndrome: report of two cases. Drut R; Galliani C Int J Surg Pathol; 2003 Jan; 11(1):25-8. PubMed ID: 12598914 [TBL] [Abstract][Full Text] [Related]
33. Further delineation of the branchio-oculo-facial syndrome. Lin AE; Gorlin RJ; Lurie IW; Brunner HG; van der Burgt I; Naumchik IV; Rumyantseva NV; Stengel-Rutkowski S; Rosenbaum K; Meinecke P Am J Med Genet; 1995 Mar; 56(1):42-59. PubMed ID: 7747785 [TBL] [Abstract][Full Text] [Related]
34. A New Case and Comprehensive Review of the Ophthalmic Manifestations of 172 Individuals With Branchio-Oculo-Facial Syndrome. Lam K; Cassidy B; Arreola R; Al Saif H; King K; Couser NL J Pediatr Ophthalmol Strabismus; 2023; 60(4):295-301. PubMed ID: 36263936 [TBL] [Abstract][Full Text] [Related]
35. Colobomatous microphthalmia with midfacial clefting: part of the spectrum of branchio-oculo-facial syndrome? Richardson E; Davison C; Moore AT Ophthalmic Genet; 1996 Jun; 17(2):59-65. PubMed ID: 8832722 [TBL] [Abstract][Full Text] [Related]
36. FOXD1 Duplication Causes Branchial Defects and Interacts with the TFAP2A Gene Implicated in the Branchio-Oculo-Facial Syndrome in Causing Eye Effects in Zebrafish. Balikova I; Devriendt K; Fryns JP; Vermeesch JR Mol Syndromol; 2010; 1(5):255-261. PubMed ID: 22140378 [TBL] [Abstract][Full Text] [Related]
37. Exclusion of the branchio-oto-renal syndrome locus (EYA1) from patients with branchio-oculo-facial syndrome. Lin AE; Semina EV; Daack-Hirsch S; Roeder ER; Curry CJ; Rosenbaum K; Weaver DD; Murray JC Am J Med Genet; 2000 Apr; 91(5):387-90. PubMed ID: 10767004 [TBL] [Abstract][Full Text] [Related]
38. Another case of preaxial polydactyly and white forelock in branchio-oculo-facial syndrome. McGaughran J Clin Dysmorphol; 2001 Jan; 10(1):67-8. PubMed ID: 11152153 [TBL] [Abstract][Full Text] [Related]