Van der Veen AY - Search Results

1

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.

Kooy RF, Van der Veen AY, Verlind E, Houwen RH, Scheffer H, Buys CH. Kooy RF, et al. Among authors: van der veen ay. Hum Genet. 1993 Jun;91(5):504-6. doi: 10.1007/BF00217780. Hum Genet. 1993. PMID: 8314565

2

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

Scheffer H, Kema IP, Kondo I, van der Veen AY, Ikeuchi T, Buys CH. Scheffer H, et al. Among authors: van der veen ay. Hum Genet. 1987 Dec;77(4):335-7. doi: 10.1007/BF00291421. Hum Genet. 1987. PMID: 2891602

3

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

van der Hout AH, van der Veen AY, Aten JA, Buys CH. van der Hout AH, et al. Among authors: van der veen ay. Hum Genet. 1988 Oct;80(2):161-4. doi: 10.1007/BF00702861. Hum Genet. 1988. PMID: 3169740

4

Ordering of polymorphic markers in the chromosome region 3p21.

van den Berg A, Kooy RF, Hulsbeek MM, de Jong D, Kok K, van der Veen AY, Buys CH. van den Berg A, et al. Among authors: van der veen ay. Cytogenet Cell Genet. 1996;72(2-3):225-8. doi: 10.1159/000134196. Cytogenet Cell Genet. 1996. PMID: 8978783

5

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

Taanman JW, van der Veen AY, Schrage C, de Vries H, Buys CH. Taanman JW, et al. Among authors: van der veen ay. Hum Genet. 1991 Jul;87(3):325-7. doi: 10.1007/BF00200913. Hum Genet. 1991. PMID: 1650756

6

Localization of amplified c-myc and n-myc in small cell lung cancer cell lines.

van der Hout AH, Kok K, van der Veen AY, Osinga J, de Leij LF, Buys CH. van der Hout AH, et al. Among authors: van der veen ay. Cancer Genet Cytogenet. 1989 Mar;38(1):1-8. doi: 10.1016/0165-4608(89)90158-1. Cancer Genet Cytogenet. 1989. PMID: 2540898

7

Defining the position of the breakpoint of the constitutional t(3;6) occurring in a family with renal cell carcinoma.

van den Berg A, van der Veen AY, Hulsbeek MM, Kovacs G, Gemmill RM, Drabkin HA, Buys CH. van den Berg A, et al. Among authors: van der veen ay. Genes Chromosomes Cancer. 1995 Mar;12(3):224-8. doi: 10.1002/gcc.2870120311. Genes Chromosomes Cancer. 1995. PMID: 7536463

8

Ordering of markers in the pericentromeric region of chromosome 10.

Hofstra RM, Stelwagen T, Pasini B, van der Veen AY, Ponder BA, Nakamura Y, Romeo G, Buys CH. Hofstra RM, et al. Among authors: van der veen ay. Hum Genet. 1995 Jul;96(1):116-8. doi: 10.1007/BF00214199. Hum Genet. 1995. PMID: 7607644

9

Identification of a tumor marker chromosome by flow sorting, DNA amplification in vitro, and in situ hybridization of the amplified product.

Boschman GA, Buys CH, van der Veen AY, Rens W, Osinga J, Slater RM, Aten JA. Boschman GA, et al. Among authors: van der veen ay. Genes Chromosomes Cancer. 1993 Jan;6(1):10-6. doi: 10.1002/gcc.2870060104. Genes Chromosomes Cancer. 1993. PMID: 7680216

10

Normal FHIT transcripts in renal cell cancer- and lung cancer-derived cell lines, including a cell line with a homozygous deletion in the FRA3B region.

van den Berg A, Draaijers TG, Kok K, Timmer T, Van der Veen AY, Veldhuis PM, de Leij L, Gerhartz CD, Naylor SL, Smith DI, Buys CH. van den Berg A, et al. Among authors: van der veen ay. Genes Chromosomes Cancer. 1997 Aug;19(4):220-7. doi: 10.1002/(sici)1098-2264(199708)19:4<220::aid-gcc3>3.0.co;2-z. Genes Chromosomes Cancer. 1997. PMID: 9258656

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