| scholarly article | Q13442814 |
| P356 | DOI | 10.1111/J.1755-3768.1990.TB01923.X |
| P698 | PubMed publication ID | 2392903 |
| P2093 | author name string | Schwartz M | |
| Rosenberg T | |||
| Simonsen SE | |||
| P2860 | cites work | Aland Island eye disease (Forsius-Eriksson syndrome) associated with contiguous deletion syndrome at Xp21. Similarity to incomplete congenital stationary night blindness | Q38671213 |
| X-linked congenital stationary night blindness. Review and report of a family with hyperopia | Q39532361 | ||
| Congenital stationary night blindness with negative electroretinogram. A new classification | Q44444809 | ||
| P433 | issue | 3 | |
| P921 | main subject | eye disease | Q3041498 |
| P304 | page(s) | 281-291 | |
| P577 | publication date | 1990-06-01 | |
| P1433 | published in | Acta ophthalmologica | Q27708761 |
| P1476 | title | Aland eye disease (Forsius-Eriksson-Miyake syndrome) with probability established in a Danish family | |
| P478 | volume | 68 |
| Q37312045 | Aland island eye disease: clinical and electrophysiological studies of a Welsh family |
| Q67854589 | Autosomal dominant stationary night-blindness A large family rediscovered |
| Q50772888 | Characterization of the ocular phenotype of Duchenne and Becker muscular dystrophy. |
| Q37560461 | Clinical Characteristics, Mutation Spectrum, and Prevalence of Åland Eye Disease/Incomplete Congenital Stationary Night Blindness in Denmark. |
| Q67854591 | Clinical and electroretinographic comparison between Åland Island eye disease and a newly found related disease with X-chromosomal inheritance |
| Q33596132 | Genetic mapping of a cone and rod dysfunction (Aland Island eye disease) to the proximal short arm of the human X chromosome. |
| Q54987446 | Spontaneous Nystagmus in the Dark in an Infantile Nystagmus Patient May Represent Negative Optokinetic Afternystagmus. |
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