Fidler C - Search Results

1

Transcription mapping of the 5q- syndrome critical region: cloning of two novel genes and sequencing, expression, and mapping of a further six novel cDNAs.

Boultwood J, Fidler C, Strickson AJ, Watkins F, Kostrzewa M, Jaju RJ, Müller U, Wainscoat JS. Boultwood J, et al. Among authors: fidler c. Genomics. 2000 May 15;66(1):26-34. doi: 10.1006/geno.2000.6193. Genomics. 2000. PMID: 10843801

2

Narrowing and genomic annotation of the commonly deleted region of the 5q- syndrome.

Boultwood J, Fidler C, Strickson AJ, Watkins F, Gama S, Kearney L, Tosi S, Kasprzyk A, Cheng JF, Jaju RJ, Wainscoat JS. Boultwood J, et al. Among authors: fidler c. Blood. 2002 Jun 15;99(12):4638-41. doi: 10.1182/blood.v99.12.4638. Blood. 2002. PMID: 12036901 Free article.

3

Chromosomal deletions in myelodysplasia.

Boultwood J, Fidler C. Boultwood J, et al. Among authors: fidler c. Leuk Lymphoma. 1995 Mar;17(1-2):71-8. doi: 10.3109/10428199509051705. Leuk Lymphoma. 1995. PMID: 7773164 Review.

4

Molecular mapping of uncharacteristically small 5q deletions in two patients with the 5q- syndrome: delineation of the critical region on 5q and identification of a 5q- breakpoint.

Boultwood J, Fidler C, Lewis S, Kelly S, Sheridan H, Littlewood TJ, Buckle VJ, Wainscoat JS. Boultwood J, et al. Among authors: fidler c. Genomics. 1994 Feb;19(3):425-32. doi: 10.1006/geno.1994.1090. Genomics. 1994. PMID: 8188284

5

Isolation of cDNAs using the YAC hybridization screen method.

Fidler C, Boultwood J. Fidler C, et al. Methods Mol Biol. 1997;68:201-10. doi: 10.1385/0-89603-482-8:201. Methods Mol Biol. 1997. PMID: 9055259 No abstract available.

6

Novel genes mapping to the critical region of the 5q- syndrome.

Boultwood J, Fidler C, Soularue P, Strickson AJ, Kostrzewa M, Jaju RJ, Cotter FE, Fairweather N, Monaco AP, Müller U, Lovett M, Jabs EW, Auffray C, Wainscoat JS. Boultwood J, et al. Among authors: fidler c. Genomics. 1997 Oct 1;45(1):88-96. doi: 10.1006/geno.1997.4899. Genomics. 1997. PMID: 9339364 Free article.

7

Molecular cytogenetic delineation of the critical deleted region in the 5q- syndrome.

Jaju RJ, Boultwood J, Oliver FJ, Kostrzewa M, Fidler C, Parker N, McPherson JD, Morris SW, Müller U, Wainscoat JS, Kearney L. Jaju RJ, et al. Among authors: fidler c. Genes Chromosomes Cancer. 1998 Jul;22(3):251-6. doi: 10.1002/(sici)1098-2264(199807)22:3<251::aid-gcc11>3.0.co;2-r. Genes Chromosomes Cancer. 1998. PMID: 9624537

8

The human POP2 gene: identification, sequencing, and mapping to the critical region of the 5q- syndrome.

Fidler C, Wainscoat JS, Boultwood J. Fidler C, et al. Genomics. 1999 Feb 15;56(1):134-6. doi: 10.1006/geno.1998.5687. Genomics. 1999. PMID: 10036195 No abstract available.

9

Physical mapping of the human ATX1 homologue (HAH1) to the critical region of the 5q- syndrome within 5q32, and immediately adjacent to the SPARC gene.

Boultwood J, Strickson AJ, Jabs EW, Cheng JF, Fidler C, Wainscoat JS. Boultwood J, et al. Among authors: fidler c. Hum Genet. 2000 Jan;106(1):127-9. doi: 10.1007/s004399900215. Hum Genet. 2000. PMID: 10982193

10

Mutation analysis of cancer using automated sequencing.

Strickson A, Fidler C. Strickson A, et al. Among authors: fidler c. Methods Mol Med. 2002;68:171-7. doi: 10.1385/1-59259-135-3:171. Methods Mol Med. 2002. PMID: 11901501 No abstract available.

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