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Year | Number of Results |
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2000 | 1 |
2003 | 2 |
2004 | 1 |
2013 | 1 |
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Page 1
The genetic basis of incomitant strabismus: consolidation of the current knowledge of the genetic foundations of disease.
Semin Ophthalmol. 2013 Sep-Nov;28(5-6):427-37. doi: 10.3109/08820538.2013.825288.
Semin Ophthalmol. 2013.
PMID: 24138051
Free PMC article.
Review.
Congenital fibrosis syndrome associated with central nervous system abnormalities.
Pieh C, Goebel HH, Engle EC, Gottlob I.
Pieh C, et al.
Graefes Arch Clin Exp Ophthalmol. 2003 Jul;241(7):546-553. doi: 10.1007/s00417-003-0703-z. Epub 2003 Jun 18.
Graefes Arch Clin Exp Ophthalmol. 2003.
PMID: 12819981
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A novel PHOX2A/ARIX mutation in an Iranian family with congenital fibrosis of extraocular muscles type 2 (CFEOM2).
Yazdani A, Chung DC, Abbaszadegan MR, Al-Khayer K, Chan WM, Yazdani M, Ghodsi K, Engle EC, Traboulsi EI.
Yazdani A, et al.
Am J Ophthalmol. 2003 Nov;136(5):861-5. doi: 10.1016/s0002-9394(03)00891-2.
Am J Ophthalmol. 2003.
PMID: 14597037
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Identification of KIF21A mutations as a rare cause of congenital fibrosis of the extraocular muscles type 3 (CFEOM3).
Yamada K, Chan WM, Andrews C, Bosley TM, Sener EC, Zwaan JT, Mullaney PB, Oztürk BT, Akarsu AN, Sabol LJ, Demer JL, Sullivan TJ, Gottlob I, Roggenkäemper P, Mackey DA, De Uzcategui CE, Uzcategui N, Ben-Zeev B, Traboulsi EI, Magli A, de Berardinis T, Gagliardi V, Awasthi-Patney S, Vogel MC, Rizzo JF 3rd, Engle EC.
Yamada K, et al.
Invest Ophthalmol Vis Sci. 2004 Jul;45(7):2218-23. doi: 10.1167/iovs.03-1413.
Invest Ophthalmol Vis Sci. 2004.
PMID: 15223798
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A clinically variant fibrosis syndrome in a Turkish family maps to the CFEOM1 locus on chromosome 12.
Sener EC, Lee BA, Turgut B, Akarsu AN, Engle EC.
Sener EC, et al.
Arch Ophthalmol. 2000 Aug;118(8):1090-7. doi: 10.1001/archopht.118.8.1090.
Arch Ophthalmol. 2000.
PMID: 10922204
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