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Ophthalmic Research, ISSN 0030-3747, 1980, Volume 12, Issue 5-6, pp. 270 - 276
The investigation of 3 families with retinitis pigmentosa (1 with autosomal dominant, two with autosomal recessive inheritance) showed no close linkage of the... 
Original Paper | Autosomal dominant retinitis pigmentosa | Autosomal recessive retinitis pigmentosa | Linkage | HLA system
Journal Article
1983, Lung biology in health and disease, ISBN 0824718666, Volume 20, xx, 516
Book
Journal of the Neurological Sciences, ISSN 0022-510X, 1984, Volume 64, Issue 2, pp. 161 - 173
Journal Article
Acta Ophthalmologica, ISSN 0001-639X, 1987, Volume 65, Issue 3, pp. 344 - 351
A diagnosis of pericentral retinal dystrophy was made in 28 patients from four families, all living in North Norway. Patients from two and three generations... 
initial stage | final stage | fluorescein angiography | autosomal dominant inheritance | pericentral retinal dystrophy | Retinal Degeneration - diagnosis | Retinal Degeneration - genetics | Humans | Middle Aged | Male | Visual Acuity | Norway | Pedigree | Visual Fields | Adolescent | Adult | Female | Aged | Child | Fluorescein Angiography
Journal Article
Acta Ophthalmologica, ISSN 0001-639X, 1987, Volume 65, Issue 2, pp. 231 - 236
A Norwegian family is reported in which two sisters and one brother all had retinitis pigmentosa with unusually late onset of clinical symptoms. The proband... 
retinitis pigmentosa | late onset | autosomal recessive inheritance | dark adaptation | electro‐retinography | Electroretinography | Pedigree | Humans | Middle Aged | Retinitis Pigmentosa - genetics | Retinitis Pigmentosa - metabolism | Female | Male | Genes, Recessive | Adaptation, Ocular | Fluorescein Angiography | Retinitis Pigmentosa - diagnosis
Journal Article
Journal Article
Journal Article
Acta Ophthalmologica, ISSN 0001-639X, 1989, Volume 67, Issue 6, pp. 703 - 709
Journal Article
Brain and Development, ISSN 0387-7604, 1989, Volume 11, Issue 2, pp. 91 - 97
The prevalence of Duchenne muscular dystrophy in the North of England (population 3.07 million) was 4.0 × 10 in 1968, 3.6 × 10 in 1979 and at least 2.3 × 10 in... 
muscular dystrophy | Prevalence | Duchenne | mortality | girls | incidence | autosomal recessive | CLINICAL NEUROLOGY | Muscular Dystrophies - epidemiology | Humans | Adolescent | Child, Preschool | England | Adult | Infant | Male | Muscular Dystrophies - genetics | Child | Muscular Dystrophies - physiopathology | Index Medicus
Journal Article
Experimental Eye Research, ISSN 0014-4835, 1990, Volume 51, Issue 4, pp. 361 - 381
Journal Article
Journal Article
Ophthalmic Genetics, ISSN 1381-6810, 1991, Volume 12, Issue 3, pp. 149 - 152
Of two brothers born of Sephardic first cousin parents one presented with congenital neural deafness, nyctalopia, visual field loss, flat ERG, unintelligible... 
ataxia | consanguinity | retinopathy | Usher syndrome | retinitis pigmentosa | myopia | nyctalopia | deafness | autosomal recessive | Deafness | Autosomal recessive | Retinopathy | Retinitis pigmentosa | Myopia | Ataxia | Consanguinity | Nyctalopia | Deafness - genetics | Vision Disorders - genetics | Humans | Adolescent | Male | Ataxia - genetics | Syndrome | Index Medicus
Journal Article
OPHTHALMIC PAEDIATRICS AND GENETICS, 09/1991, Volume 12, Issue 3, pp. 149 - 152
Of two brothers born of Sephardic first cousin parents one presented with congenital neural deafness, nyctalopia, visual field loss, flat ERG, unintelligible... 
USHER SYNDROME | NYCTALOPIA | AUTOSOMAL RECESSIVE | MYOPIA | OPHTHALMOLOGY | RETINOPATHY | PEDIATRICS | DEAFNESS | ATAXIA | CONSANGUINITY | RETINITIS-PIGMENTOSA
Journal Article
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