Reply to Inglehearn.

Yazar: Bergen, A A, Pinckers, A J
Baskı/Yayın Bilgisi 1998

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

Yazar: Bergen, A A, Pinckers, A J
Baskı/Yayın Bilgisi 1997

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

Yazar: Bergen, A A, Kestelyn, P, Leys, M, Meire, F
Baskı/Yayın Bilgisi 1994

Global gene expression profiling of ischemic preconditioning in the rat retina

Yazar: Kamphuis, W., Dijk, F., van Soest, S., Bergen, A.A.B.
Baskı/Yayın Bilgisi 2007

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

Yazar: Arveiler, B, Hofker, M H, Bergen, A A, Mandel, J L
Baskı/Yayın Bilgisi 1987

Efficient DNA carrier detection in X linked juvenile retinoschisis.

Yazar: Bergen, A A, ten Brink, J B, van Schooneveld, M J
Baskı/Yayın Bilgisi 1995

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

Yazar: Meire, F M, Bergen, A A, De Rouck, A, Leys, M, Delleman, J W
Baskı/Yayın Bilgisi 1994

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

Yazar: Bergen, A A, ten Brink, J B, Bleeker-Wagemakers, L M, van Schooneveld, M J
Baskı/Yayın Bilgisi 1994

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

Yazar: Bergen, A A, ten Brink, J B, Riemslag, F, Schuurman, E J, Meire, F, Tijmes, N, de Jong, P T
Baskı/Yayın Bilgisi 1996

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

Yazar: Assink, J J, Tijmes, N T, ten Brink, J B, Oostra, R J, Riemslag, F C, de Jong, P T, Bergen, A A
Baskı/Yayın Bilgisi 1997

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

Yazar: Hofker, M H, Skraastad, M I, Bergen, A A, Wapenaar, M C, Bakker, E, Millington-Ward, A, van Ommen, G J, Pearson, P L
Baskı/Yayın Bilgisi 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...

Yazar: 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
Baskı/Yayın Bilgisi 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.

Yazar: 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.
Yayımlandı 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...

Yazar: 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
Baskı/Yayın Bilgisi 1999