| scholarly article | Q13442814 |
| P356 | DOI | 10.1016/0888-7543(91)90315-6 |
| P698 | PubMed publication ID | 2071141 |
| P2093 | author name string | Schwartz M | |
| Rosenberg T | |||
| P433 | issue | 2 | |
| P921 | main subject | eye disease | Q3041498 |
| P304 | page(s) | 327-332 | |
| P577 | publication date | 1991-06-01 | |
| P1433 | published in | Genomics | Q5533503 |
| P1476 | title | Aland eye disease: linkage data | |
| P478 | volume | 10 |
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| Q33596132 | Genetic mapping of a cone and rod dysfunction (Aland Island eye disease) to the proximal short arm of the human X chromosome. |
| Q42659278 | Identification of a key recombinant which assigns the incomplete congenital stationary night blindness gene proximal to MAOB. |
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| Q24312225 | The electroretinographic diagnosis of the incomplete form of congenital stationary night blindness |
| Q35196313 | Xp21 contiguous gene syndromes: deletion quantitation with bivariate flow karyotyping allows mapping of patient breakpoints |
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