Kok K - Search Results

1

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. J Med Genet. 1999 Apr;36(4):346-7. J Med Genet. 1999. PMID: 10227409 Free PMC article. No abstract available.

2

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: kok k. 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

3

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: kok k. Cytogenet Cell Genet. 1996;72(2-3):225-8. doi: 10.1159/000134196. Cytogenet Cell Genet. 1996. PMID: 8978783

4

A comparison of genomic structures and expression patterns of two closely related flanking genes in a critical lung cancer region at 3p21.3.

Timmer T, Terpstra P, van den Berg A, Veldhuis PM, Ter Elst A, Voutsinas G, Hulsbeek MM, Draaijers TG, Looman MW, Kok K, Naylor SL, Buys CH. Timmer T, et al. Among authors: kok k. Eur J Hum Genet. 1999 May-Jun;7(4):478-86. doi: 10.1038/sj.ejhg.5200334. Eur J Hum Genet. 1999. PMID: 10352938

5

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: kok k. 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

6

Inclusion of new microsatellite repeats in allelic loss analysis excludes retention of heterozygosity in the renal cell carcinoma critical region in 3p21.

Kok K, Draaijers TG, Mosselaar A, de Jong D, Buys CH. Kok K, et al. Cancer Genet Cytogenet. 2000 Jan 1;116(1):40-3. doi: 10.1016/s0165-4608(99)00094-1. Cancer Genet Cytogenet. 2000. PMID: 10616530

7

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: kok k. Cancer Genet Cytogenet. 1989 Mar;38(1):1-8. doi: 10.1016/0165-4608(89)90158-1. Cancer Genet Cytogenet. 1989. PMID: 2540898

8

Application of a comprehensive subtelomere array in clinical diagnosis of mental retardation.

Kok K, Dijkhuizen T, Swart YE, Zorgdrager H, van der Vlies P, Fehrmann R, te Meerman GJ, Gerssen-Schoorl KB, van Essen T, Sikkema-Raddatz B, Buys CH. Kok K, et al. Eur J Med Genet. 2005 Jul-Sep;48(3):250-62. doi: 10.1016/j.ejmg.2005.04.007. Eur J Med Genet. 2005. PMID: 16179221

9

Partial 3q duplication syndrome and assignment of D3S5 to 3q25-3q28.

van Essen AJ, Kok K, van den Berg A, de Jong B, Stellink F, Bos AF, Scheffer H, Buys CH. van Essen AJ, et al. Among authors: kok k. Hum Genet. 1991 Jun;87(2):151-4. doi: 10.1007/BF00204171. Hum Genet. 1991. PMID: 2066102 Review.

10

Direct molecular analysis of a deletion of 3p in tumors from patients with sporadic renal cell carcinoma.

van der Hout AH, Kok K, van den Berg A, Oosterhuis JW, Carritt B, Buys CH. van der Hout AH, et al. Among authors: kok k. Cancer Genet Cytogenet. 1988 Jun;32(2):281-5. doi: 10.1016/0165-4608(88)90292-0. Cancer Genet Cytogenet. 1988. PMID: 2835149

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