Callen DF - Search Results

1

Dinucleotide repeat polymorphism at D16S533.

Cleton-Jansen AM, Moerland HW, Vossen RH, Callen DF, Breuning MH, Devilee P. Cleton-Jansen AM, et al. Among authors: callen df. Hum Mol Genet. 1994 Jan;3(1):216. doi: 10.1093/hmg/3.1.216. Hum Mol Genet. 1994. PMID: 8162043 No abstract available.

2

Chromosome 16 microdeletion in a patient with juvenile neuronal ceroid lipofuscinosis (Batten disease).

Taschner PE, de Vos N, Thompson AD, Callen DF, Doggett N, Mole SE, Dooley TP, Barth PG, Breuning MH. Taschner PE, et al. Among authors: callen df. Am J Hum Genet. 1995 Mar;56(3):663-8. Am J Hum Genet. 1995. PMID: 7887420 Free PMC article.

3

Mapping of the breast basic conserved gene (D16S444E) to human chromosome band 16q24.3.

Cleton-Jansen AM, Moerland HW, Callen DF, Doggett NA, Devilee P, Cornelisse CJ. Cleton-Jansen AM, et al. Among authors: callen df. Cytogenet Cell Genet. 1995;68(1-2):49-51. doi: 10.1159/000133886. Cytogenet Cell Genet. 1995. PMID: 7956357

4

Map of 16 polymorphic loci on the short arm of chromosome 16 close to the polycystic kidney disease gene (PKD1).

Breuning MH, Snijdewint FG, Brunner H, Verwest A, Ijdo JW, Saris JJ, Dauwerse JG, Blonden L, Keith T, Callen DF, et al. Breuning MH, et al. Among authors: callen df. J Med Genet. 1990 Oct;27(10):603-13. doi: 10.1136/jmg.27.10.603. J Med Genet. 1990. PMID: 1978860 Free PMC article.

5

At least two different regions are involved in allelic imbalance on chromosome arm 16q in breast cancer.

Cleton-Jansen AM, Moerland EW, Kuipers-Dijkshoorn NJ, Callen DF, Sutherland GR, Hansen B, Devilee P, Cornelisse CJ. Cleton-Jansen AM, et al. Among authors: callen df. Genes Chromosomes Cancer. 1994 Feb;9(2):101-7. doi: 10.1002/gcc.2870090205. Genes Chromosomes Cancer. 1994. PMID: 7513539

6

Probe, VK5B, is located in the same interval as the autosomal dominant adult polycystic kidney disease locus, PKD1.

Hyland VJ, Suthers GK, Friend K, MacKinnon RN, Callen DF, Breuning MH, Keith T, Brown VA, Phipps P, Sutherland GR. Hyland VJ, et al. Among authors: callen df. Hum Genet. 1990 Feb;84(3):286-8. doi: 10.1007/BF00200577. Hum Genet. 1990. PMID: 1968038

7

Report of the fourth international workshop on human chromosome 16 mapping 1995.

Doggett NA, Breuning MH, Callen DF. Doggett NA, et al. Among authors: callen df. Cytogenet Cell Genet. 1996;72(4):271-93. doi: 10.1159/000134205. Cytogenet Cell Genet. 1996. PMID: 8641131 No abstract available.

8

Genomic structure and expression analysis of the spastic paraplegia gene, SPG7.

Settasatian C, Whitmore SA, Crawford J, Bilton RL, Cleton-Jansen AM, Sutherland GR, Callen DF. Settasatian C, et al. Among authors: callen df. Hum Genet. 1999 Jul-Aug;105(1-2):139-44. doi: 10.1007/s004399900087. Hum Genet. 1999. PMID: 10480368

9

Loss of heterozygosity mapping at chromosome arm 16q in 712 breast tumors reveals factors that influence delineation of candidate regions.

Cleton-Jansen AM, Callen DF, Seshadri R, Goldup S, Mccallum B, Crawford J, Powell JA, Settasatian C, van Beerendonk H, Moerland EW, Smit VT, Harris WH, Millis R, Morgan NV, Barnes D, Mathew CG, Cornelisse CJ. Cleton-Jansen AM, et al. Among authors: callen df. Cancer Res. 2001 Feb 1;61(3):1171-7. Cancer Res. 2001. PMID: 11221848

10

Mutation analysis of the Fanconi anaemia A gene in breast tumours with loss of heterozygosity at 16q24.3.

Cleton-Jansen AM, Moerland EW, Pronk JC, van Berkel CG, Apostolou S, Crawford J, Savoia A, Auerbach AD, Mathew CG, Callen DF, Cornelisse CJ. Cleton-Jansen AM, et al. Among authors: callen df. Br J Cancer. 1999 Mar;79(7-8):1049-52. doi: 10.1038/sj.bjc.6690168. Br J Cancer. 1999. PMID: 10098735 Free PMC article.

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