Reply to Inglehearn.

nork Bergen, A A, Pinckers, A J
Argitaratua 1998

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

nork Bergen, A A, Pinckers, A J
Argitaratua 1997

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

nork Bergen, A A, Kestelyn, P, Leys, M, Meire, F
Argitaratua 1994

Global gene expression profiling of ischemic preconditioning in the rat retina

nork Kamphuis, W., Dijk, F., van Soest, S., Bergen, A.A.B.
Argitaratua 2007

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

nork Arveiler, B, Hofker, M H, Bergen, A A, Mandel, J L
Argitaratua 1987

Efficient DNA carrier detection in X linked juvenile retinoschisis.

nork Bergen, A A, ten Brink, J B, van Schooneveld, M J
Argitaratua 1995

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

nork Meire, F M, Bergen, A A, De Rouck, A, Leys, M, Delleman, J W
Argitaratua 1994

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

nork Bergen, A A, ten Brink, J B, Bleeker-Wagemakers, L M, van Schooneveld, M J
Argitaratua 1994

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

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

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

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

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

nork Hofker, M H, Skraastad, M I, Bergen, A A, Wapenaar, M C, Bakker, E, Millington-Ward, A, van Ommen, G J, Pearson, P L
Argitaratua 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...

nork 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
Argitaratua 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.

nork 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.
Argitaratua izan da 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...

nork 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
Argitaratua 1999