Flynn HC - Search Results

1

Development of a dual-color, double fusion FISH assay to detect RPN1/EVI1 gene fusion associated with inv(3), t(3;3), and ins(3;3) in patients with myelodysplasia and acute myeloid leukemia.

Shearer BM, Sukov WR, Flynn HC, Knudson RA, Ketterling RP. Shearer BM, et al. Among authors: flynn hc. Am J Hematol. 2010 Aug;85(8):569-74. doi: 10.1002/ajh.21746. Am J Hematol. 2010. PMID: 20556821 Free article. Clinical Trial.

2

Development of a D-FISH method to detect DEK/CAN fusion resulting from t(6;9)(p23;q34) in patients with acute myelogenous leukemia.

Shearer BM, Knudson RA, Flynn HC, Ketterling RP. Shearer BM, et al. Among authors: flynn hc. Leukemia. 2005 Jan;19(1):126-31. doi: 10.1038/sj.leu.2403557. Leukemia. 2005. PMID: 15510206

3

Interphase FISH to detect PBX1/E2A fusion resulting from the der(19)t(1;19)(q23;p13.3) or t(1;19)(q23;p13.3) in paediatric patients with acute lymphoblastic leukaemia.

Shearer BM, Flynn HC, Knudson RA, Ketterling RP. Shearer BM, et al. Among authors: flynn hc. Br J Haematol. 2005 Apr;129(1):45-52. doi: 10.1111/j.1365-2141.2005.05415.x. Br J Haematol. 2005. PMID: 15801954 Free article.

4

Novel FISH probes designed to detect IGK-MYC and IGL-MYC rearrangements in B-cell lineage malignancy identify a new breakpoint cluster region designated BVR2.

Einerson RR, Law ME, Blair HE, Kurtin PJ, McClure RF, Ketterling RP, Flynn HC, Dogan A, Remstein ED. Einerson RR, et al. Among authors: flynn hc. Leukemia. 2006 Oct;20(10):1790-9. doi: 10.1038/sj.leu.2404340. Epub 2006 Aug 3. Leukemia. 2006. PMID: 16888615

5

CHIC2 deletion, a surrogate for FIP1L1-PDGFRA fusion, occurs in systemic mastocytosis associated with eosinophilia and predicts response to imatinib mesylate therapy.

Pardanani A, Ketterling RP, Brockman SR, Flynn HC, Paternoster SF, Shearer BM, Reeder TL, Li CY, Cross NC, Cools J, Gilliland DG, Dewald GW, Tefferi A. Pardanani A, et al. Among authors: flynn hc. Blood. 2003 Nov 1;102(9):3093-6. doi: 10.1182/blood-2003-05-1627. Epub 2003 Jul 3. Blood. 2003. PMID: 12842979 Free article.

6

Microduplication 22q11.2, an emerging syndrome: clinical, cytogenetic, and molecular analysis of thirteen patients.

Ensenauer RE, Adeyinka A, Flynn HC, Michels VV, Lindor NM, Dawson DB, Thorland EC, Lorentz CP, Goldstein JL, McDonald MT, Smith WE, Simon-Fayard E, Alexander AA, Kulharya AS, Ketterling RP, Clark RD, Jalal SM. Ensenauer RE, et al. Among authors: flynn hc. Am J Hum Genet. 2003 Nov;73(5):1027-40. doi: 10.1086/378818. Epub 2003 Oct 2. Am J Hum Genet. 2003. PMID: 14526392 Free PMC article.

7

FIP1L1-PDGFRA fusion: prevalence and clinicopathologic correlates in 89 consecutive patients with moderate to severe eosinophilia.

Pardanani A, Brockman SR, Paternoster SF, Flynn HC, Ketterling RP, Lasho TL, Ho CL, Li CY, Dewald GW, Tefferi A. Pardanani A, et al. Among authors: flynn hc. Blood. 2004 Nov 15;104(10):3038-45. doi: 10.1182/blood-2004-03-0787. Epub 2004 Jul 29. Blood. 2004. PMID: 15284118 Free article.

8

Familial 22q11.2 deletions in DiGeorge/velocardiofacial syndrome are predominantly smaller than the commonly observed 3Mb.

Adeyinka A, Stockero KJ, Flynn HC, Lorentz CP, Ketterling RP, Jalal SM. Adeyinka A, et al. Among authors: flynn hc. Genet Med. 2004 Nov-Dec;6(6):517-20. doi: 10.1097/01.gim.0000144011.97407.b6. Genet Med. 2004. PMID: 15545748

9

Connective tissue dysplasia in five new patients with NF1 microdeletions: further expansion of phenotype and review of the literature.

Mensink KA, Ketterling RP, Flynn HC, Knudson RA, Lindor NM, Heese BA, Spinner RJ, Babovic-Vuksanovic D. Mensink KA, et al. Among authors: flynn hc. J Med Genet. 2006 Feb;43(2):e8. doi: 10.1136/jmg.2005.034256. J Med Genet. 2006. PMID: 16467218 Free PMC article. Review.

10

Splenic small B-cell lymphoma with IGH/BCL3 translocation.

Soma LA, Gollin SM, Remstein ED, Ketterling RP, Flynn HC, Rajasenan KK, Swerdlow SH. Soma LA, et al. Among authors: flynn hc. Hum Pathol. 2006 Feb;37(2):218-30. doi: 10.1016/j.humpath.2005.09.025. Hum Pathol. 2006. PMID: 16426923 Review.

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