Reply to Inglehearn.

Por Bergen, A A, Pinckers, A J
Publicado em 1998

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

Por Bergen, A A, Pinckers, A J
Publicado em 1997

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

Por Bergen, A A, Kestelyn, P, Leys, M, Meire, F
Publicado em 1994

Paucity of signs in X linked ocular albinism with a 700 kb deletion spanning the OA1 gene

Por TIJMES, N., BERGEN, A., DE JONG, P. T V M
Publicado em 1998

Global gene expression profiling of ischemic preconditioning in the rat retina

Por Kamphuis, W., Dijk, F., van Soest, S., Bergen, A.A.B.
Publicado em 2007

The polydeoxyadenylate tract of Alu repetitive elements is polymorphic in the human genome.

Por Economou, E P, Bergen, A W, Warren, A C, Antonarakis, S E
Publicado em 1990

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

Por Arveiler, B, Hofker, M H, Bergen, A A, Mandel, J L
Publicado em 1987

Efficient DNA carrier detection in X linked juvenile retinoschisis.

Por Bergen, A A, ten Brink, J B, van Schooneveld, M J
Publicado em 1995

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

Por Meire, F M, Bergen, A A, De Rouck, A, Leys, M, Delleman, J W
Publicado em 1994

Correlation of population parameters leading to power differences in association studies with population stratification

Por HE, Y., JIANG, R., FU, W., BERGEN, A. W., SWAN, G. E., JIN, L.
Publicado em 2008

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

Por Bergen, A A, ten Brink, J B, Bleeker-Wagemakers, L M, van Schooneveld, M J
Publicado em 1994

Sorsby fundus dystrophy without a mutation in the TIMP-3 gene

Por Assink, J., de Backer, E., ten, B, Kohno, T., de Jong, P. T V M, Bergen, A., Meire, F.
Publicado em 2000

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

Por Bergen, A A, ten Brink, J B, Riemslag, F, Schuurman, E J, Meire, F, Tijmes, N, de Jong, P T
Publicado em 1996

Identification of mutations in the AIPL1, CRB1, GUCY2D, RPE65, and RPGRIP1 genes in patients with juvenile retinitis pigmentosa

Por Booij, J, Florijn, R, ten, B, Loves, W, Meire, F, van Schooneveld, M J, de Jong, P T., Bergen, A
Publicado em 2005

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

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

Dual origins of Finns revealed by Y chromosome haplotype variation.

Por Kittles, R A, Perola, M, Peltonen, L, Bergen, A W, Aragon, R A, Virkkunen, M, Linnoila, M, Goldman, D, Long, J C
Publicado em 1998

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

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

Por 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
Publicado em 1987

Dopamine D(2) Receptor Polymorphisms and Adenoma Recurrence in the Polyp Prevention Trial

Por Murphy, G., Cross, A.J., Sansbury, L.S., Bergen, A., Laiyemo, A.O., Albert, P.S., Wang, Z., Yu, B., Schatzkin, A., Lehman, T., Kalidindi, A., Modali, R., Schatzkin, A., Lanza, E.
Publicado em 2009

Ancestral Asian source(s) of new world Y-chromosome founder haplotypes.

Por Karafet, T M, Zegura, S L, Posukh, O, Osipova, L, Bergen, A, Long, J, Goldman, D, Klitz, W, Harihara, S, de Knijff, P, Wiebe, V, Griffiths, R C, Templeton, A R, Hammer, M F
Publicado em 1999