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遗传性视网膜脱离:附二家系 被引量:1

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作者 宋方 靳明华
出处 《眼底病》 CSCD 1991年第3期167-168,共2页
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  • 1Cuendet JF, Gailloud C, Dufour R. Genetics and idiopathic retinal detachment. Mod Probl Ophthalmol, 1975, 15:10-21.
  • 2Theelen T, Go SL, Tilanus MA, et al. Autosomal dominant rhegmatogenous retinal detachment- clinical appearance and surgical outcome. Graefe's Arch Clin Exp Ophthalmol, 2004, 242:892 - 897.
  • 3左假.医学遗传学(第4版)[M].人民卫生出版社,2004.53-60.
  • 4Scott JD. Duke - Elder lecture. prevention and perspective in retinal detachment. Eye, 1989, 3:491-515.
  • 5Seery CM, Pruett RC, Liberfarb RM, et al. Distinctive cataract in theSticklersyndrome. AmJ Ophthalmol, 1990, 110: 143-148.
  • 6Nielson CE. Stickler's syndrome. Acta Ophthalmol, 1981, 59:286 - 295.
  • 7Maumenee IH. Vitreoretinal degeneration as a sign of generalized connective tissue diseases. Am J Ophthalmol, 1979, 88: 432-449.
  • 8Snead MP, Payne SJ, Barton DE, et al. Stickler syndrome:correlation between vitreoretinal phenotypes and linkage to COL 2A1. Eye, 1994, 8:609-614.
  • 9Snead MP, Yates JR, Pope FM, et al. Masked confirmation of linkage between pe 1 congenital vitreous anomaly and COL 2A1 in Stickler syndrome. Graefe's Arch Clin Exp Ophthalmol, 1996,234: 720- 721.
  • 10Mcleod D, Black G, Bishop PN. Vitrous phenotype: genotype correlation in Stickler syndrome. Grafe's Arch Clin Exp Ophthalmol, 2002, 240: 63-65.

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