Genetic mapping of a cone and rod dysfunction (Aland Island eye disease) to the proximal short arm of the human X chromosome.

Author:

Glass I A,Good P,Coleman M P,Fullwood P,Giles M G,Lindsay S,Nemeth A H,Davies K E,Willshaw H A,Fielder A

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference13 articles.

1. Congenital stationary night blindness. In: Krill's hereditary retinal and choroidal diseases;Krill, A.,1977

2. ERG in a case of Xchromosomal pigment deficiency of fundus in combination with myopia, dyschromatopsia and defective dark-adaption;Elenius, V.; Eriksson, A.; Forsius, H.,1966

3. Aland eye disease (Forsius Eriksson-Miyake syndrome) with probability established in a Danish family;Rosenberg, T.; Schwartz, M.; Simonsen, S.E.;Acta Ophthalniol,1990

4. Aland eye disease: no albino misrouting;DB, Van Dorp; AW, Eriksson; JW, Dellman;Clin Genet,1985

5. Some notes on publications of Professor Arnold Sorsby and on Aland eye disease (Forsius-Eriksson syndrome);Waardenberg, P.J.;I Med Genet,1970

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