A. V. Veen

发表

Region with a Marked Instability in Yeast Artificial Chromosomes

K. Kok, E. Schoenmakers, C. Buys, 1994 .

Localization at a subband level of polymorphic 13q14 DNA probes for diagnosis of hereditary retinoblastoma and Wilson disease

H. Scheffer, I. Kondo, I. Kema, 1987, Human Genetics.

Limited impact of multiple 5′ single-nucleotide polymorphisms on the transcriptional control of the human β2-adrenoceptor gene

H. Jansen, E. Wierenga, R. Westland, 2004, Immunogenetics.

Deletion of a DNA sequence at the chromosomal region 3p21 in all major types of lung cancer

J. Osinga, K. Kok, P. Postmus, 1987, Nature.

Assignment of the gene coding for human cytochrome c oxidase subunit VIb to chromosome 19, band q13.1, by fluorescence in situ hybridisation

J. Taanman, C. Buys, C. Schrage, 1991, Human Genetics.

Localization of DNA probes with tight linkage to the cystic fibrosis locus by in situ hybridization using fibroblasts with a 7q22 deletion

J. Aten, C. Buys, A. Hout, 1988, Human Genetics.

Physical localisation of the chromosomal marker D13S31 places the Wilson disease locus at the junction of bands q14.3 and q21.1 of chromosome 13

H. Scheffer, R. Kooy, R. Houwen, 1993, Human Genetics.

Ordering of markers in the pericentromeric region of chromosome 10

B. Ponder, Yusuke Nakamura, R. Hofstra, 1995, Human Genetics.