Authors: Smith, A St Heaps, L Sharma, P Jarvis, A Forsyth, C

Citation: A. Smith et al., 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, CANC GENET, 130(1), 2001, pp. 29-32

Authors: Smith, A Robson, L St Heaps, L Sharma, P Dunlop, L Bhave, A Bradstock, K

Citation: A. Smith et al., 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, CANC GENET, 129(2), 2001, pp. 173-176

Authors: Sharma, P Jarvis, A Jauch, A St Heaps, L Shaw, P Smith, A

Citation: P. Sharma et al., Complex variant t(4;11) characterized by fluorescence in situ hybridization in infant acute lymphoblastic leukemia, CANC GENET, 127(2), 2001, pp. 177-180

Authors: St Heaps, L Robson, L Smith, A

Citation: L. St Heaps et al., Review of referrals for the FISH detection of Williams syndrome highlightsthe importance of testing in supravalvular aortic stenosis pulmonary stenosis, AM J MED G, 98(1), 2001, pp. 109-111

Authors: Smith, A Jauch, A St Heaps, L Robson, L Kearney, B

Citation: A. Smith et al., Unbalanced translocation t(15;22) in 'severe' Prader-Willi syndrome, ANN GENET, 43(3-4), 2000, pp. 125-130