van der Veen AY - Search Results

1

FISH and array-CGH analysis of a complex chromosome 3 aberration suggests that loss of CNTN4 and CRBN contributes to mental retardation in 3pter deletions.

Dijkhuizen T, van Essen T, van der Vlies P, Verheij JB, Sikkema-Raddatz B, van der Veen AY, Gerssen-Schoorl KB, Buys CH, Kok K. Dijkhuizen T, et al. Among authors: van der veen ay. Am J Med Genet A. 2006 Nov 15;140(22):2482-7. doi: 10.1002/ajmg.a.31487. Am J Med Genet A. 2006. PMID: 17036314

2

Breakpoint mapping by FISH in a Sotos patient with a constitutional translocation t(3;6).

Kok K, Mosselaar A, Faber H, Dijkhuizen T, Draaijers TG, van der Veen AY, Buys CH, Schrander-Stumpel CT. Kok K, et al. Among authors: van der veen ay. J Med Genet. 1999 Apr;36(4):346-7. J Med Genet. 1999. PMID: 10227409 Free PMC article. No abstract available.

3

Tetrasomy 9p due to an intrachromosomal triplication of 9p13-p22.

Verheij JB, Bouman K, van Lingen RA, van Lookeren Campagne JG, Leegte B, van der Veen AY, Hofstra RM, Buys CH, van Essen AJ. Verheij JB, et al. Among authors: van der veen ay. Am J Med Genet. 1999 Sep 10;86(2):168-73. doi: 10.1002/(sici)1096-8628(19990910)86:2<168::aid-ajmg16>3.0.co;2-q. Am J Med Genet. 1999. PMID: 10449655 Review.

4

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

5

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

6

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

7

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

8

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

9

An evolutionary rearrangement of the Xp11.3-11.23 region in 3p21.3, a region frequently deleted in a variety of cancers.

Timmer T, Terpstra P, van den Berg A, Veldhuis PM, Ter Elst A, van der Veen AY, Kok K, Naylor SL, Buys CH. Timmer T, et al. Among authors: van der veen ay. Genomics. 1999 Sep 1;60(2):238-40. doi: 10.1006/geno.1999.5878. Genomics. 1999. PMID: 10486216

10

RFP2, c13ORF1, and FAM10A4 are the most likely tumor suppressor gene candidates for B-cell chronic lymphocytic leukemia.

van Everdink WJ, Baranova A, Lummen C, Tyazhelova T, Looman MW, Ivanov D, Verlind E, Pestova A, Faber H, van der Veen AY, Yankovsky N, Vellenga E, Buys CH. van Everdink WJ, et al. Among authors: van der veen ay. Cancer Genet Cytogenet. 2003 Oct 1;146(1):48-57. doi: 10.1016/s0165-4608(03)00126-2. Cancer Genet Cytogenet. 2003. PMID: 14499696

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