Molecular cytogeneticsKEARNEY, Lyndal.Baillière's best practice & research. Clinical haematology. 2001, Vol 14, Num 3, pp 645-668, issn 1521-6926Article

Cytogenetics in haematologyBUCKLE, Veronica J; KEARNEY, Lyndal.Baillière's best practice & research. Clinical haematology. 2001, Vol 14, Num 3, issn 1521-6926, 210 p.Serial Issue

The clinical significance of cytogenetic abnormalities in acute myeloid leukaemiaGRIMWADE, David.Baillière's best practice & research. Clinical haematology. 2001, Vol 14, Num 3, pp 497-529, issn 1521-6926Article

Childhood myeloid leukaemiasHALL, Georgina W.Baillière's best practice & research. Clinical haematology. 2001, Vol 14, Num 3, pp 573-591, issn 1521-6926Article

Acute lymphoblastic leukaemiaHARRISON, Christine J.Baillière's best practice & research. Clinical haematology. 2001, Vol 14, Num 3, pp 593-607, issn 1521-6926Article

Chromosome instability syndromesTAYLOR, A. M. R.Baillière's best practice & research. Clinical haematology. 2001, Vol 14, Num 3, pp 631-644, issn 1521-6926Article

The cytogenetics of myelodysplastic syndromesOLNEY, Harold J; LE BEAU, Michelle M.Baillière's best practice & research. Clinical haematology. 2001, Vol 14, Num 3, pp 479-495, issn 1521-6926Article

Lymphoid neoplasmsOSCIER, David Graham; GARDINER, Anne Catherine.Baillière's best practice & research. Clinical haematology. 2001, Vol 14, Num 3, pp 609-630, issn 1521-6926Article

Cytogenetics of chronic myeloid leukaemiaCHASE, Andrew; HUNTLY, Brian J. P; CROSS, Nicholas C. P et al.Baillière's best practice & research. Clinical haematology. 2001, Vol 14, Num 3, pp 553-571, issn 1521-6926Article

Genetic variegation of clonal architecture and propagating cells in leukaemiaANDERSON, Kristina; LUTZ, Christoph; KEARNEY, Lyndal et al.Nature (London). 2011, Vol 469, Num 7330, pp 356-361, issn 0028-0836, 6 p.Article

A cryptic t(5;11)(q35;p15.5) in 2 children with acute myeloid leukemia with apparently normal karyotypes, identified by a multiplex fluorescence in situ hybridization telomere assayBROWN, Jill; JAWAD, Mays; TWIGG, Stephen R. F et al.Blood. 2002, Vol 99, Num 7, pp 2526-2531, issn 0006-4971Article

Acquisition of genome-wide copy number alterations in monozygotic twins with acute lymphoblastic leukemiaBATEMAN, Caroline M; COLMAN, Susan M; HAIN, Richard et al.Blood. 2010, Vol 115, Num 17, pp 3553-3558, issn 0006-4971, 6 p.Article

Myeloproliferative disordersBENCH, Anthony J; CROSS, Nicholas C. P; HUNTLY, Brian J. P et al.Baillière's best practice & research. Clinical haematology. 2001, Vol 14, Num 3, pp 531-551, issn 1521-6926Article

A novel gene, NSD1, is fused to NUP98 in the t(5;1 1)(q35;p15.5) in de novo childhood acute myeloid leukemiaJAJU, Rina J; FIDLER, Carrie; BOULTWOOD, Jacqueline et al.Blood. 2001, Vol 98, Num 4, pp 1264-1267, issn 0006-4971Article

Cytogenetic and molecular evidence of marrow involvement in extramedullary acute myeloid leukaemiaLILLINGTON, Debra M; JAJU, Rina J; SHANKAR, A. G et al.British journal of haematology. 2000, Vol 110, Num 3, pp 547-551, issn 0007-1048Article

Specific JAK2 mutation (JAK2R683) and multiple gene deletions in Down syndrome acute lymphoblastic leukemiaKEARNEY, Lyndal; GONZALEZ DE CASTRO, David; HARRISON, Christine J et al.Blood. 2009, Vol 113, Num 3, pp 646-648, issn 0006-4971, 3 p.Article

Narrowing and genomic annotation of the commonly deleted region of the 5q- syndromeBOULTWOOD, Jacqueline; FIDLER, Carrie; WAINSCOAT, James S et al.Blood. 2002, Vol 99, Num 12, pp 4638-4641, issn 0006-4971Article

Study of 30 patients with unexplained developmental delay and dysmorphic features or congenital abnormalities using conventional cytogenetics and multiplex FISH telomere (M-TEL) integrity assayPOPP, Susanne; SCHULZE, Birgit; KEARNEY, Lyndal et al.Human genetics. 2002, Vol 111, Num 1, pp 31-39, issn 0340-6717Article

The paired box domain gene PAX5 is fused to ETV6/TEL in an acute lymphoblastic leukemia caseCAZZANIGA, Giovanni; DANIOTTI, Maria; TOSI, Sabrina et al.Cancer research (Baltimore). 2001, Vol 61, Num 12, pp 4666-4670, issn 0008-5472Article

A new strategy for the detection of subtelomeric rearrangementsFAUTH, Christine; HONGEN ZHANG; SPEICHER, Michael R et al.Human genetics. 2001, Vol 109, Num 6, pp 576-583, issn 0340-6717Article

Clonal origins of relapse in ETV6-RUNX1 acute lymphoblastic leukemiaVAN DELFT, Frederik W; HORSLEY, Sharon; FORD, Anthony et al.Blood. 2011, Vol 117, Num 23, pp 6247-6254, issn 0006-4971, 8 p.Article

Deregulated expression of cytokine receptor gene, CRLF2, is involved in lymphoid transformation in B-cell precursor acute lymphoblastic leukemiaRUSSELL, Lisa J; CAPASSO, Melania; GUTTERY, David S et al.Blood. 2009, Vol 114, Num 13, pp 2688-2698, issn 0006-4971, 11 p.Article

Array comparative genome hybridization analysis of acute lymphoblastic leukaemia and acute megakaryoblastic leukaemia in patients with Down syndromeLO, Ken C; CHALKER, Jane; STREHL, Sabine et al.British journal of haematology. 2008, Vol 142, Num 6, pp 934-945, issn 0007-1048, 12 p.Article

Sequence, structure and pathology of the fully annotated terminal 2 Mb of the short arm of human chromosome 16DANIELS, Rachael J; PEDEN, John F; HIGGS, Douglas R et al.Human molecular genetics (Print). 2001, Vol 10, Num 4, pp 339-352, issn 0964-6906Article