Colour vision, ophthalmological and linkage studies in a pedigree with a tritan defect.
作者信息
Went L N, Völker-Dieben H, de Vries-de Mol E C
出版信息
Mod Probl Ophthalmol. 1974;13(0):272-6.
PMID:4548144
Abstract
摘要
相似文献
1
Colour vision, ophthalmological and linkage studies in a pedigree with a tritan defect.一个伴有蓝色色盲缺陷家系的色觉、眼科及连锁研究
Mod Probl Ophthalmol. 1974;13(0):272-6.
2
Comparative colour vision and other ophthalmological studies in three families with dominant inherited juvenile optic atrophy.三个显性遗传青少年视神经萎缩家族的比较色觉及其他眼科研究。
Mod Probl Ophthalmol. 1974;13(0):277-81.
3
Congenital tritanopia without neuroretinal disease.无神经视网膜疾病的先天性蓝色色盲
Invest Ophthalmol. 1973 Aug;12(8):608-17.
4
Colour vision in a pedigree with autosomal dominant optic atrophy.一个患有常染色体显性遗传性视神经萎缩的家系中的色觉情况
Mod Probl Ophthalmol. 1976;17:315-9.
5
The AN-59 anomaloscope in the research of acquired colour vision deficiencies.用于后天性色觉缺陷研究的AN-59色盲检查镜
Mod Probl Ophthalmol. 1972;11:34-9.
6
Color vision in dominant optic atrophy.显性视神经萎缩中的色觉
J Clin Neuroophthalmol. 1992 Jun;12(2):98-103.
7
Japanese family with blue cone monochromatism.患有蓝色视锥细胞单色症的日裔家庭。
Jpn J Ophthalmol. 1992;36(2):132-41.
8
Acquired deficiency of colour vision in lateral homonymous hemianopsia.同侧偏盲性后天性色觉缺陷
Mod Probl Ophthalmol. 1972;11:150-9.
9
Studies on color vision anomalies in subjects with alcoholism.酗酒者色觉异常的研究。
Ann Ophthalmol. 1973 Dec;5(12):1277-92.
10
Farnsworth-Munsell 100-hue test for patients with diabetes mellitus.糖尿病患者的 Farnsworth-Munsell 100 色觉试验
Ann Ophthalmol. 1992 Jun;24(6):205-8.
引用本文的文献
1
The genetics of tritan disturbances.蓝色色盲的遗传学
Hum Genet. 1985;69(3):255-62. doi: 10.1007/BF00293036.
Zotero 插件