Reply to Inglehearn.

af Bergen, A A, Pinckers, A J
Udgivet 1998

Localization of a novel X-linked progressive cone dystrophy gene to Xq27: evidence for genetic heterogeneity.

af Bergen, A A, Pinckers, A J
Udgivet 1997

Identification of a key recombinant which assigns the incomplete congenital stationary night blindness gene proximal to MAOB.

af Bergen, A A, Kestelyn, P, Leys, M, Meire, F
Udgivet 1994

Global gene expression profiling of ischemic preconditioning in the rat retina

af Kamphuis, W., Dijk, F., van Soest, S., Bergen, A.A.B.
Udgivet 2007

A PstI RFLP detected by probe cpX73 (DXS159) in Xq11-q12.

af Arveiler, B, Hofker, M H, Bergen, A A, Mandel, J L
Udgivet 1987

Efficient DNA carrier detection in X linked juvenile retinoschisis.

af Bergen, A A, ten Brink, J B, van Schooneveld, M J
Udgivet 1995

X linked progressive cone dystrophy. Localisation of the gene locus to Xp21-p11.1 by linkage analysis.

af Meire, F M, Bergen, A A, De Rouck, A, Leys, M, Delleman, J W
Udgivet 1994

Refinement of the chromosomal position of the X linked juvenile retinoschisis gene.

af Bergen, A A, ten Brink, J B, Bleeker-Wagemakers, L M, van Schooneveld, M J
Udgivet 1994

Conclusive evidence for a distinct congenital stationary night blindness locus in Xp21.1.

af Bergen, A A, ten Brink, J B, Riemslag, F, Schuurman, E J, Meire, F, Tijmes, N, de Jong, P T
Udgivet 1996

A gene for X-linked optic atrophy is closely linked to the Xp11.4-Xp11.2 region of the X chromosome.

af Assink, J J, Tijmes, N T, ten Brink, J B, Oostra, R J, Riemslag, F C, de Jong, P T, Bergen, A A
Udgivet 1997

The X chromosome shows less genetic variation at restriction sites than the autosomes.

af Hofker, M H, Skraastad, M I, Bergen, A A, Wapenaar, M C, Bakker, E, Millington-Ward, A, van Ommen, G J, Pearson, P L
Udgivet 1986

Efficient isolation of X chromosome-specific single-copy probes from a cosmid library of a human X/hamster hybrid-cell line: mapping of new probes close to the locus for X-linked m...

af Hofker, M H, Bergen, A A, Skraastad, M I, Carpenter, N J, Veenema, H, Connor, J M, Bakker, E, van Ommen, G J, Pearson, P L
Udgivet 1987

Stem Cell Derived Retinal Pigment Epithelium: The Role of Pigmentation as Maturation Marker and Gene Expression Profile Comparison with Human Endogenous Retinal Pigment Epithelium.

af Bennis, A., Jacobs, J. G., Catsburg, L. A. E., ten Brink, J. B., Koster, C., Schlingemann, R. O., van Meurs, J., Gorgels, T. G. M. F., Moerland, P. D., Heine, V. M., Bergen, A. A.
Udgivet i Stem Cell Rev (2017)

The 2588G-->C mutation in the ABCR gene is a mild frequent founder mutation in the Western European population and allows the classification of ABCR mutations in patients with Star...

af Maugeri, A, van Driel, M A, van de Pol, D J, Klevering, B J, van Haren, F J, Tijmes, N, Bergen, A A, Rohrschneider, K, Blankenagel, A, Pinckers, A J, Dahl, N, Brunner, H G, Deutman, A F, Hoyng, C B, Cremers, F P
Udgivet 1999