Smith A - Search Results

1

17p- syndrome arising from a novel dicentric translocation in a patient with acute myeloid leukemia.

Watson N, Dunlop L, Robson L, Sharma P, Smith A. Watson N, et al. Among authors: smith a. Cancer Genet Cytogenet. 2000 Apr 15;118(2):159-62. doi: 10.1016/s0165-4608(99)00188-0. Cancer Genet Cytogenet. 2000. PMID: 10748299

2

Novel chromosome 16 abnormality--der(16)del(16) (q13)t(16;21)(p11.2;q22)--associated with acute myeloid leukemia.

Sharma P, Watson N, Robson L, Gallo J, Smith A. Sharma P, et al. Among authors: smith a. Cancer Genet Cytogenet. 1999 Aug;113(1):25-8. doi: 10.1016/s0165-4608(99)00008-4. Cancer Genet Cytogenet. 1999. PMID: 10459342

3

Frequency of trisomy 15 and loss of the Y chromosome in adult leukemia.

Smith A, Watson N, Sharma P. Smith A, et al. Cancer Genet Cytogenet. 1999 Oct 15;114(2):108-11. doi: 10.1016/s0165-4608(99)00042-4. Cancer Genet Cytogenet. 1999. PMID: 10549265

4

Two children with acute lymphoblastic leukemia and "jumping" translocations: both involve 1q23 as the donor breakpoint.

Jarvis A, Sharma P, Watson N, Smith A. Jarvis A, et al. Among authors: smith a. Cancer Genet Cytogenet. 1999 Oct 15;114(2):112-6. doi: 10.1016/s0165-4608(99)00044-8. Cancer Genet Cytogenet. 1999. PMID: 10549266 Review.

5

Novel translocation t(3;11)(p21;q24) in multiple myeloma characterised by FISH.

Smith A, de Lambert R, Robson L. Smith A, et al. Ann Genet. 1999;42(4):221-4. Ann Genet. 1999. PMID: 10674162

6

A novel dicentric deleted chromosome 21 arising from tandem translocation.

Robinson L, Robson L, Sharma P, Watson N, Hertzberg M, Smith A. Robinson L, et al. Among authors: smith a. Cancer Genet Cytogenet. 2000 Sep;121(2):208-11. doi: 10.1016/s0165-4608(00)00247-8. Cancer Genet Cytogenet. 2000. PMID: 11063810

7

Fifteen cases of t(1;19)(q23;p13.3) identified in an Australian series of 122 children and 80 adults with acute lymphoblastic leukemia.

Sharma P, Watson N, Sartor M, McCowage G, Smith A. Sharma P, et al. Among authors: smith a. Cancer Genet Cytogenet. 2001 Jan 15;124(2):132-6. doi: 10.1016/s0165-4608(00)00333-2. Cancer Genet Cytogenet. 2001. PMID: 11172904

8

Complex variant t(4;11) characterized by fluorescence in situ hybridization in infant acute lymphoblastic leukemia.

Sharma P, Jarvis A, Jauch A, St Heaps L, Shaw P, Smith A. Sharma P, et al. Among authors: smith a. Cancer Genet Cytogenet. 2001 Jun;127(2):177-80. doi: 10.1016/s0165-4608(00)00439-8. Cancer Genet Cytogenet. 2001. PMID: 11425460

9

Routine fluorescence in situ hybridization with the MLL probe does not reliably detect two separate signals on one chromosome 11 in patients with trisomy 11.

Smith A, Robson L, Heaps LS, Sharma P, Dunlop L, Bhave A, Bradstock K. Smith A, et al. Cancer Genet Cytogenet. 2001 Sep;129(2):173-6. doi: 10.1016/s0165-4608(01)00449-6. Cancer Genet Cytogenet. 2001. PMID: 11566351 Clinical Trial.

10

Abnormal dicentric chromosome with co-amplification of sequences from chromosomes 11 and 19: a novel rearrangement in a patient with myelodysplastic syndrome transforming to acute myeloid leukemia.

Smith A, Heaps LS, Sharma P, Jarvis A, Forsyth C. Smith A, et al. Cancer Genet Cytogenet. 2001 Oct 1;130(1):29-32. doi: 10.1016/s0165-4608(01)00463-0. Cancer Genet Cytogenet. 2001. PMID: 11672770

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