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.
43. Epiblepharon outcomes: comparing apples and oranges. Tan P; Malhotra R Br J Ophthalmol; 2018 Nov; 102(11):1483-1484. PubMed ID: 30348679 [No Abstract] [Full Text] [Related]
44. Characterization of the ocular findings in the nablus masklike facial syndrome. Lance S; Wong G; Young D J AAPOS; 2016 Oct; 20(5):457-459. PubMed ID: 27647115 [TBL] [Abstract][Full Text] [Related]
45. Excision of distichiasis eyelashes through a tarsoconjunctival trapdoor. Dortzbach RK; Butera RT Arch Ophthalmol; 1978 Jan; 96(1):111-2. PubMed ID: 623539 [TBL] [Abstract][Full Text] [Related]
46. [Basic principles of lid reconstruction]. Schmid E Klin Monbl Augenheilkd; 1973 Mar; 162(3):296-305. PubMed ID: 4197397 [No Abstract] [Full Text] [Related]
47. Prognosis of upper eyelid epiblepharon repair in Down syndrome. Gupta VP; Gupta R; Gupta P Am J Ophthalmol; 2011 Jun; 151(6):1104; author reply 1104-5. PubMed ID: 21616215 [No Abstract] [Full Text] [Related]
49. Sclerocornea, hypertelorism, syndactyly, and ambiguous genitalia. Martínez-Frías ML; Bermejo E; Sánchez Otero T; Urioste M; Morena V; Cruz E Am J Med Genet; 1994 Jan; 49(2):195-7. PubMed ID: 8116666 [TBL] [Abstract][Full Text] [Related]
50. Prognosis of upper eyelid epiblepharon repair in down syndrome. Lee KM; Choung HK; Kim NJ; Lee MJ; Lee KW; Khwarg SI Am J Ophthalmol; 2010 Oct; 150(4):476-480.e1. PubMed ID: 20643394 [TBL] [Abstract][Full Text] [Related]
51. [Apropos of a case of incomplete cryptophthalmos]. Ba EA; Ndiaye MR; Wade A; Ndiaye PA; Ndoye NB; Ndiaye CS; Ndoye PA Dakar Med; 1996; 41(1):59-61. PubMed ID: 9827095 [TBL] [Abstract][Full Text] [Related]
52. Malformative syndrome with cryptophthalmia. Francois J Int Ophthalmol Clin; 1968; 8(4):817-37. PubMed ID: 4313811 [No Abstract] [Full Text] [Related]
53. Fraser and Ablepharon macrostomia phenotypes: concurrence in one family and association with mutated FRAS1. Cavalcanti DP; Matejas V; Luquetti D; Mello MF; Zenker M Am J Med Genet A; 2007 Feb; 143A(3):241-7. PubMed ID: 17163535 [TBL] [Abstract][Full Text] [Related]