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KERD
논문KCI 등재

선천 안진을 동반한 터너증후군

Congenital Nystagmus in Turner Syndrome

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참고문헌 (7)

  1. Ranke MB, "Turner's syndrome", Lancet, 358, pp.309~314 (2001)[DOI]
  2. Brunnerova R, "Ocular manifestations in Turner's syndrome", Ceska Slov Oftalmol, 63, pp.176~184 (2007)
  3. Wikiera B, "The presence of eye defects in patients with Turner syndrome is irrespective of their karyotype", Clin Endocrinol(Oxf), 83, pp.842~848 (2015)[DOI]
  4. Clement-Jones M, "The short stature homeobox gene SHOX is involved in skeletal abnormalities in Turner syndrome", Human Mol Genet, 9, pp.695~702 (2000)[DOI]
  5. Noma T, "Stage-and sex-dependent expressions of Usp9x, an X-linked mouse ortholog of Drosophila Fat facets, during gonadal development and oogenesis in mice", Mech Dev, 119, pp.S91~S95 (2002)[DOI]
  6. Schorderet DF, "Novel mutations in FRMD7 in X-linked congenital nystagmus", Hum Mutat, 28, pp.525~ (2007)
  7. Kerrison JB, "Clinical and genetic analysis of a family with X-linked congenital nystagmus (NYS1)", Ophthalmic Genet, 22, pp.241~248 (2001)[DOI]

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