Thompson PW - Search Results

1

Human T-cell tumours containing chromosome 14 inversion or translocation with breakpoints proximal to immunoglobulin joining regions at 14q32.

Mengle-Gaw L, Willard HF, Smith CI, Hammarström L, Fischer P, Sherrington P, Lucas G, Thompson PW, Baer R, Rabbitts TH. Mengle-Gaw L, et al. Among authors: thompson pw. EMBO J. 1987 Aug;6(8):2273-80. doi: 10.1002/j.1460-2075.1987.tb02501.x. EMBO J. 1987. PMID: 3117531 Free PMC article.

2

Variant translocation (3;inv(16)) in acute myelomonocytic leukemia with eosinophilia.

Thompson PW, Lucas GS, Davies MF, Whittaker JA. Thompson PW, et al. Cancer Genet Cytogenet. 1991 Sep;55(2):269-71. doi: 10.1016/0165-4608(91)90089-d. Cancer Genet Cytogenet. 1991. PMID: 1933831 No abstract available.

3

A new variant of chromosome 16.

Thompson PW, Roberts SH. Thompson PW, et al. Hum Genet. 1987 May;76(1):100-1. doi: 10.1007/BF00283058. Hum Genet. 1987. PMID: 3570297

4

Red cell dimorphism in a young man with a constitutional chromosomal translocation t(11;22)(p15.5;q11.21).

Rees MI, Worwood M, Thompson PW, Gilbertson C, May A. Rees MI, et al. Among authors: thompson pw. Br J Haematol. 1994 Jun;87(2):386-95. doi: 10.1111/j.1365-2141.1994.tb04927.x. Br J Haematol. 1994. PMID: 7947283

5

Characterization of psu dic(6;5)(p21.3;q13) with reverse chromosome painting in a patient with secondary myelodysplastic syndrome following treatment for multiple myeloma.

Lee-Jones L, Ramsahoye B, Booth M, Thompson P, Whittaker J, Hoy T. Lee-Jones L, et al. Cancer Genet Cytogenet. 2004 Jan 1;148(1):49-54. doi: 10.1016/s0165-4608(03)00218-8. Cancer Genet Cytogenet. 2004. PMID: 14697641

6

Replication studies in the 16p+ variant.

Thompson PW, Roberts SH, Rees SM. Thompson PW, et al. Hum Genet. 1990 Mar;84(4):371-2. doi: 10.1007/BF00196238. Hum Genet. 1990. PMID: 2307461

7

The genetics of a small autosomal region of Drosophila melanogaster containing the structural gene for alcohol dehydrogenase. VII. Characterization of the region around the snail and cactus loci.

Ashburner M, Thompson P, Roote J, Lasko PF, Grau Y, el Messal M, Roth S, Simpson P. Ashburner M, et al. Genetics. 1990 Nov;126(3):679-94. doi: 10.1093/genetics/126.3.679. Genetics. 1990. PMID: 2123463 Free PMC article.

8

A cytogenetic deletion, del(17)(q11.22q21.1), in a patient with sporadic neurofibromatosis type 1 (NF1) associated with dysmorphism and developmental delay.

Upadhyaya M, Roberts SH, Maynard J, Sorour E, Thompson PW, Vaughan M, Wilkie AO, Hughes HE. Upadhyaya M, et al. Among authors: thompson pw. J Med Genet. 1996 Feb;33(2):148-52. doi: 10.1136/jmg.33.2.148. J Med Genet. 1996. PMID: 8929953 Free PMC article.

9

Wiskott-Aldrich syndrome: no evidence of chromosome instability.

Thompson P, Standen GR. Thompson P, et al. Cancer Genet Cytogenet. 1993 Aug;69(1):22-4. doi: 10.1016/0165-4608(93)90106-v. Cancer Genet Cytogenet. 1993. PMID: 8374895

10

Translocation 3;21 in Philadelphia chromosome positive chronic myeloid leukemia at diagnosis.

Thompson PW, Whittaker JA. Thompson PW, et al. Cancer Genet Cytogenet. 1989 Jun;39(2):143-6. doi: 10.1016/0165-4608(89)90178-7. Cancer Genet Cytogenet. 1989. PMID: 2752367

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