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Archives of Ophthalmology, ISSN 0003-9950, 07/1968, Volume 80, Issue 1, pp. 68 - 76
Three adults with macular dysfunction and peripheral pigmentary retinal degeneration are described as one clinical entity called progressive cone-rod... 
Electroretinography | Darkness | Humans | Color | Macula Lutea - physiopathology | Male | Genes, Recessive | Adaptation, Ocular | Eye Diseases - diagnosis | Retinal Pigments - physiology | Eye Diseases - genetics | Photoreceptor Cells - physiopathology | Laurence-Moon Syndrome | Vision, Ocular | Light | Adult | Flicker Fusion | Index Medicus | Abridged Index Medicus
Journal Article
Archives of Ophthalmology, ISSN 0003-9950, 02/1969, Volume 81, Issue 2, pp. 215 - 225
Journal Article
Vision Research, ISSN 0042-6989, 1970, Volume 10, Issue 8, pp. 717 - 743
The examination results of the tritanomal, Mrs. F., whose father is a tritan subdichromat, and of her closest relatives are described in detail in view of the... 
Eye Diseases - complications | Humans | Middle Aged | Male | Sex Chromosomes | Genes, Recessive | Color Vision Defects - genetics | Color Vision Defects - congenital | Pedigree | Adult | Female | Heterozygote | Aged | Color Perception Tests | Index Medicus
Journal Article
The New England Journal of Medicine, ISSN 0028-4793, 12/1970, Volume 283, Issue 26, pp. 1466 - 1468
Journal Article
Journal Article
American Journal of Ophthalmology, ISSN 0002-9394, 1971, Volume 72, Issue 2, pp. 332 - 341
The coincidence of inverse retinitis pigmentosa, deafness, and hypogenitalism was found in three siblings. The patients, a man, age 62 years, and two women,... 
OPHTHALMOLOGY | Electroretinography | Deafness - genetics | Audiometry | Humans | Middle Aged | Menarche | Retinitis Pigmentosa - genetics | Male | Olfaction Disorders | Sex Characteristics | Genes, Recessive | Dark Adaptation | Hypogonadism - genetics | Visual Fields | Karyotyping | Adult | Female | Color Perception | Fundus Oculi | Scotoma - genetics
Journal Article
Birth defects original article series, ISSN 0547-6844, 03/1971, Volume 7, Issue 4, pp. 52 - 63
Journal Article
Birth defects original article series, ISSN 0547-6844, 03/1971, Volume 7, Issue 3, pp. 99 - 116
The sex-linked chorioretinal heredodegenerations are progressive chorioretinal degeneration or choroideremia, sex-linked pigmentary retinopathy and sex-linked... 
Albinism - diagnosis | Humans | Child, Preschool | Infant | Male | Sex Chromosomes | Atrophy | Genes, Dominant | Visual Fields | Adult | Female | Child | Electroretinography | Diagnosis, Differential | Retinal Degeneration - genetics | Retinitis Pigmentosa - genetics | Choroid | Visual Acuity | Genes, Recessive | Sclerosis - genetics | Eye Diseases - genetics | Pedigree | Heterozygote | Visual Perception | Fundus Oculi
Journal Article
Birth defects original article series, ISSN 0547-6844, 03/1971, Volume 7, Issue 3, pp. 180 - 182
Journal Article
Birth defects original article series, ISSN 0547-6844, 03/1971, Volume 7, Issue 3, pp. 83 - 98
1) Dystrophia retinae dysacusis syndrome: Two different recessively inherited forms have been observed among 133 cases diagnosed in Finland--a country with a... 
Retinal Diseases - genetics | Deafness - genetics | Gait | Humans | Middle Aged | Child, Preschool | Retinitis Pigmentosa - genetics | Infant | Male | Retinal Diseases - congenital | Sex Chromosomes | Melanosis - congenital | Genes, Recessive | Syndrome | Macular Degeneration - genetics | Pedigree | Adolescent | Finland | Sex Factors | Adult | Female | Child | Melanosis - genetics
Journal Article
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