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.
338 related articles for article (PubMed ID: 8291545)
1. Blepharophimosis, ptosis, and epicanthus inversus syndrome (BPES) associated with interstitial deletion of band 3q22: review and gene assignment to the interface of band 3q22.3 and 3q23. Jewett T; Rao PN; Weaver RG; Stewart W; Thomas IT; Pettenati MJ Am J Med Genet; 1993 Dec; 47(8):1147-50. PubMed ID: 8291545 [TBL] [Abstract][Full Text] [Related]
2. Blepharophimosis, ptosis, epicanthus inversus syndrome, a new case associated with de novo balanced autosomal translocation [46,XY,t(3;7)(q23;q32)]. Boccone L; Meloni A; Falchi AM; Usai V; Cao A Am J Med Genet; 1994 Jul; 51(3):258-9. PubMed ID: 8074155 [TBL] [Abstract][Full Text] [Related]
3. Refinement of a translocation breakpoint associated with blepharophimosis-ptosis-epicanthus inversus syndrome to a 280-kb interval at chromosome 3q23. Toomes C; Dixon MJ Genomics; 1998 Nov; 53(3):308-14. PubMed ID: 9799597 [TBL] [Abstract][Full Text] [Related]
4. Molecular cytogenetic evaluation in a patient with a translocation (3;21) associated with blepharophimosis, ptosis, epicanthus inversus syndrome (BPES). Praphanphoj V; Goodman BK; Thomas GH; Niel KM; Toomes C; Dixon MJ; Geraghty MT Genomics; 2000 Apr; 65(1):67-9. PubMed ID: 10777667 [TBL] [Abstract][Full Text] [Related]
5. Blepharophimosis, ptosis, and epicanthus inversus syndrome (BPES) and microcephaly. Ishikiriyama S; Goto M Am J Med Genet; 1994 Aug; 52(2):245. PubMed ID: 7802022 [No Abstract] [Full Text] [Related]
6. Deletion 3q in two patients with blepharophimosis-ptosis-epicanthus inversus syndrome (BPES). Costa T; Pashby R; Huggins M; Teshima IE J Pediatr Ophthalmol Strabismus; 1998; 35(5):271-6. PubMed ID: 9782438 [TBL] [Abstract][Full Text] [Related]
7. Blepharophimosis-ptosis-epicanthus inversus syndrome plus: deletion 3q22.3q23 in a patient with characteristic facial features and with genital anomalies, spastic diplegia, and speech delay. Zahanova S; Meaney B; Łabieniec B; Verdin H; De Baere E; Nowaczyk MJM Clin Dysmorphol; 2012 Jan; 21(1):48-52. PubMed ID: 21934608 [TBL] [Abstract][Full Text] [Related]
8. Acquired microcephaly in blepharophimosis-ptosis-epicanthus inversus syndrome because of an interstitial 3q22.3q23 deletion. Dean SJ; Holden KR; Dwivedi A; Dupont BR; Lyons MJ Pediatr Neurol; 2014 Jun; 50(6):636-9. PubMed ID: 24725350 [TBL] [Abstract][Full Text] [Related]
10. Boy with a chromosome del (3)(q12q23) and blepharophimosis syndrome. Fujita H; Meng J; Kawamura M; Tozuka N; Ishii F; Tanaka N Am J Med Genet; 1992 Nov; 44(4):434-6. PubMed ID: 1442882 [TBL] [Abstract][Full Text] [Related]
12. Further evidence for the location of the blepharophimosis syndrome (BPES) at 3q22.3-q23. Fryns JP; Strømme P; van den Berghe H Clin Genet; 1993 Sep; 44(3):149-51. PubMed ID: 8275574 [TBL] [Abstract][Full Text] [Related]
14. Definition of the blepharophimosis, ptosis, epicanthus inversus syndrome critical region at chromosome 3q23 based on the analysis of chromosomal anomalies. Lawson CT; Toomes C; Fryer A; Carette MJ; Taylor GM; Fukushima Y; Dixon MJ Hum Mol Genet; 1995 May; 4(5):963-7. PubMed ID: 7633459 [TBL] [Abstract][Full Text] [Related]
15. A gene for blepharophimosis-ptosis-epicanthus inversus syndrome maps to chromosome 3q23. Amati P; Chomel JC; Nivelon-Chevalier A; Gilgenkrantz S; Kitzis A; Kaplan J; Bonneau D Hum Genet; 1995 Aug; 96(2):213-5. PubMed ID: 7635472 [TBL] [Abstract][Full Text] [Related]
16. Genetic analysis of a five generation Indian family with BPES: a novel missense mutation (p.Y215C). Kumar A; Babu M; Raghunath A; Venkatesh CP Mol Vis; 2004 Jul; 10():445-9. PubMed ID: 15257268 [TBL] [Abstract][Full Text] [Related]
17. De novo interstitial deletion of 3q22.3-q25.2 encompassing FOXL2, ATR, ZIC1, and ZIC4 in a patient with blepharophimosis/ptosis/epicanthus inversus syndrome, Dandy-Walker malformation, and global developmental delay. Lim BC; Park WY; Seo EJ; Kim KJ; Hwang YS; Chae JH J Child Neurol; 2011 May; 26(5):615-8. PubMed ID: 21471554 [TBL] [Abstract][Full Text] [Related]
18. Closing in on the BPES gene on 3q23: mapping of a de Novo reciprocal translocation t(3;4)(q23;p15.2) breakpoint within a 45-kb cosmid and mapping of three candidate genes, RBP1, RBP2, and beta'-COP, distal to the breakpoint. De Baere E; Van Roy N; Speleman F; Fukushima Y; De Paepe A; Messiaen L Genomics; 1999 Apr; 57(1):70-8. PubMed ID: 10191085 [TBL] [Abstract][Full Text] [Related]
19. Mutation analysis of the FOXL2 gene in Chinese patients with blepharophimosis-ptosis-epicanthus inversus syndrome. Tang S; Wang X; Lin L; Sun Y; Wang Y; Yu H Mutagenesis; 2006 Jan; 21(1):35-9. PubMed ID: 16394030 [TBL] [Abstract][Full Text] [Related]