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Clinical and linkage study on a consanguineous Chinese family with autosomal recessive high myopia

By Zhikuan Yang, Xueshan Xiao, Shiqiang Li and Qingjiong Zhang
Topics: Research Article
Publisher: Molecular Vision
OAI identifier: oai:pubmedcentral.nih.gov:2635848
Provided by: PubMed Central

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Citations

  1. (2002). A genome wide scan for familial high myopia suggests a novel locus on chromosome 7q36.
  2. (2003). A look at slowing progression of myopia. Lancet
  3. (2005). A new locus for autosomal dominant high myopia maps to 4q22-q27 between D4S1578 and D4S1612.
  4. (2008). A review of current approaches to identifying human genes involved in myopia. Clin Exp Optom
  5. (1998). A second locus for familial high myopia maps to chromosome 12q.
  6. (1991). Autosomal recessive inheritance of myopia in Hong Kong Chinese infants. Ophthalmic Physiol Opt
  7. (1994). Avoiding recomputation in linkage analysis. Hum Hered
  8. (2007). Complex trait genetics of refractive error.
  9. (2007). Confirmation of a genetic locus for X-linked recessive high myopia outside MYP1.
  10. (1984). Easy calculations of lod scores and genetic risks on small computers.
  11. (2008). Evaluation of EGR1 as a candidate gene for high myopia. Mol Vis
  12. (2005). Evaluation of Lipin 2 as a candidate gene for autosomal dominant 1 high-grade myopia. Gene
  13. (1998). Evidence that a locus for familial high myopia maps to chromosome 18p.
  14. (2007). Exclusion of transforming growth factor-beta1 as a candidate gene for myopia in the Japanese.
  15. (2009). Further refinement of the MYP2 locus for autosomal dominant high myopia by linkage TABLE 3. TWO-POINT LINKAGE RESULTS FOR MARKERS AT 14Q22.1-Q24.2. Position LOD score at θ= cM*
  16. (1995). Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results.
  17. (2009). Genetic epidemiology study of pathological myopia. Zhonghua Yi Xue Yi Chuan Xue Za Zhi 2000; 17:178-80. [PMID: 10837519] Molecular Vision
  18. (2007). Genetic linkage study of high-grade myopia in a Hutterite population from South Dakota. Mol Vis
  19. (2008). Genome-wide Scan Maps a Novel High Myopia Locus to 5p15. Invest Ophthalmol Vis Sci
  20. (2003). Genomewide homozygosity mapping and molecular analysis of a candidate gene located on 22q13 (fibulin-1) in a previously undescribed vitreoretinal dystrophy. Arch Ophthalmol
  21. (2005). Genomic structure and organization of the high grade Myopia-2 locus (MYP2) critical region: mutation screening of 9 positional candidate genes. Mol Vis
  22. (2003). Homozygosity mapping of a Desbuquois dysplasia locus to chromosome 17q25.3.
  23. (2005). How genetic is school myopia? Prog Retin Eye Res
  24. (2005). Identification of a novel locus on 2q for autosomal dominant high-grade myopia. Invest Ophthalmol Vis Sci
  25. (2004). incidence, and progression of myopia of school children in Hong Kong. Invest Ophthalmol Vis Sci
  26. (1975). Influence of the myopia gene on brain development. Clin Genet
  27. (2003). Interactions of genes and environment in myopia. Dev Ophthalmol
  28. (2004). Linkage analysis of the genetic loci for high myopia on 18p,
  29. (2007). Mutations in NYX of individuals with high myopia, but without night blindness. Mol Vis
  30. Myopia and vision
  31. (2003). New locus for autosomal dominant high myopia maps to the long arm of chromosome 17. Invest Ophthalmol Vis Sci
  32. Novel locus for X linked recessive high myopia maps to
  33. (2005). Pedigree study of pathological myopia. Yi Chuan Xue Bao
  34. (2008). Refinement of the MYP3 locus on human chromosome 12 in a German family with Mendelian autosomal dominant high-grade myopia by SNP array mapping.
  35. (2004). Sequence variants in the transforming growth beta-induced factor (TGIF) gene are not associated with high myopia. Invest Ophthalmol Vis Sci
  36. (2004). Standard for clinical electroretinography
  37. (1999). VISION 2020-the right to sight: from strategies to action.
  38. (2004). X-linked high myopia associated with cone dysfunction. Arch Ophthalmol
  39. (1990). X-linked myopia: Bornholm eye disease. Linkage to DNA markers on the distal part of Xq. Clin Genet

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