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Payne, AM., Khaliq, S., Hameed, A., Ismail, M., Bessant, DAR., Mehdi, SQ. and Bhattacharya, SS. et al. (1999) 'Localisation of a gene for autosomal recessive cone-rod dystrophy to chromosome'. Investigative Ophthalmology and Visual Science, 40 (4). pp. 16624 - 16624. ISSN: 1552-5783

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Themis, M., Forbes, SJ., Chan, L., Cooper, RG., Etheridge, CJ., Miller, AD., Hodgson, HJ. and Coutelle, C. et al. (1998) 'Enhanced in vitro and in vivo gene delivery using cationic agent complexed retrovirus vectors'. Gene Therapy, 5 (9). pp. 1180 - 1186. ISSN: 0969-7128

Slijepcevic, P. (1998) 'Telomere length and telomere-centromere relationships?'.4th International Symposium on Chromosomal Aberrations. UNIV ESSEN, ESSEN, GERMANY. 3 - 29 August. Elsevier BV. pp. 215 - 220. ISSN: 0027-5107

Roberts, T., Chernova, O. and Cowell, JK. (1998) 'NB4S, a member of the TBC1 domain family of genes, is truncated as a result of a constitutional t(1;10)(p22;q21) chromosome translocation in a patient with stage 4S neuroblastoma'. Human Molecular Genetics, 7 (7). pp. 1169 - 1178. ISSN: 0964-6906

Kelsell, RE., Gregory-Evans, K., Payne, AM., Perrault, I., Kaplan, J., Yang, RB., Garbers, DL., Bird, AC., Moore, AT. and Hunt, DM. et al. (1998) 'Mutations in the retinal guanylate cyclase (RETGC-1) gene in dominant cone-rod dystrophy'. Human Molecular Genetics, 7 (7). pp. 1179 - 1184. ISSN: 0964-6906

King, JA., Bridger, JM., Löchelt, M., Lichter, P., Schulz, TF., Schirrmacher, V. and Khazaie, K. et al. (1998) 'Nucleocytoplasmic transport of HTLV-1 RNA is regulated by two independent LTR encoded nuclear retention elements'. Oncogene, 16 (25). pp. 3309 - 3316. ISSN: 0950-9232

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Slijepcevic, P. (1998) 'Telomeres and mechanisms of Robertsonian fusion'. Chromosoma, 107 (2). pp. 136 - 140. ISSN: 0009-5915

Elliott, DJ., Oghene, K., Makarov, G., Makarova, O., Hargreave, TB., Chandley, AC., Eperon, IC. and Cooke, HJ. et al. (1998) 'Dynamic changes in the subnuclear organisation of pre-mRNA splicing proteins and RBM during human germ cell development'. Journal of Cell Science, 111 (9). pp. 1255 - 1265. ISSN: 0021-9533

Slijepcevic, P. and Bryant, PE. (1998) 'Chromosome healing, telomere capture and mechanisms of radiation- induced chromosome breakage'. International Journal of Radiation Biology, 73 (1). pp. 1 - 13. ISSN: 0955-3002

Karteris, E., Grammatopoulos, D., Dai, Y., Olah, KB., Ghobara, TB., Easton, A. and Hillhouse, EW. et al. (1998) 'The human placenta and fetal membranes express the corticotropin-releasing hormone receptor 1alpha (CRH-1alpha) and the CRH-C variant receptor.'. J Clin Endocrinol Metab, 83 (4). pp. 1376 - 1379. ISSN: 0021-972X

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Höfken, T., Linder, D., Kleene, R., Göke, B. and Wagner, ACC. (1998) 'Regulation of pancreatic membrane dipeptidase mRNA expression and identification as zymogen granule membrane protein by peptide sequencing'. Elsevier BV. pp. A469 - A469. ISSN: 0016-5085

Papaioannou, M., Payne, AM., Rougas, C., Bessant, D., Loutradis-Anagnostou, A., Balassopoulou, A. and Bhattacharya, S. et al. (1998) 'Mutation screening in the photoreceptor-specific gene (CRX) in patients of Greek origin'. Investigative Ophthalmology and Visual Science, 39 (4). ISSN: 1552-5783

Woodcock, SC., Raux, EC., Evans, A., Dalvin, ST., Payne, AM., Downes, SM., Bird, AC., Bhattacharya, SS., Hunt, DM. and Warren, MJ. et al. (1998) 'Characterization of the Y99C mutant of a guanylate cyclase activator protein 1 (GCAP1)'. Investigative Ophthalmology and Visual Science, 39 (4). ISSN: 1552-5783

Slijepcevic, P. and Bryant, PE. (1998) 'Reply to J. P. Murnane's Letter to the Editor'. Radiation Research, 149 (3). pp. 310 - 310. ISSN: 0033-7587

Tosi, S., Giudici, G., Mosna, G., Harbott, J., Specchia, G., Grosveld, G., Prìvitera, E., Kearney, L., Biondi, A. and Cazzaniga, G. et al. (1998) 'Identification of new partner chromosomes involved in fusions with the ETV6 (TEL) gene in hematologic malignancies'. Genes Chromosomes and Cancer, 21 (3). pp. 223 - 229. ISSN: 1045-2257

Slijepcevic, P., Natarajan, AT. and Bryant, PE. (1998) 'Telomeres and radiation-induced chromosome breakage'. Mutagenesis, 13 (1). pp. 45 - 49. ISSN: 0267-8357

Payne, AM., Downes, SM., Bessant, DAR., Taylor, R., Holder, GE., Warren, MJ., Bird, AC. and Bhattacharya, SS. et al. (1998) 'A mutation in guanylate cyclase activator 1A(GUCA1A) in an autosomal dominant cone dystrophy pedigree mapping to a new locus on chromosome 6p21.1'. Human Molecular Genetics, 7 (2). pp. 273 - 277. ISSN: 0964-6906

Sokal, I., Li, N., Surgucheva, I., Warren, MJ., Payne, AM., Bhattacharya, SS., Baehr, W. and Palczewski, K. et al. (1998) 'GCAP1(Y99C) mutant is constitutively active in autosomal dominant cone dystrophy'. Molecular Cell, 2 (1). pp. 129 - 133. ISSN: 1097-2765

Papaioannou, M., Bessant, D., Payne, A., Bellingham, J., Rougas, C., Loutradis-Anagnostou, A., Gregory-Evans, C., Balassopoulou, A. and Bhattacharya, S. et al. (1998) 'A new family of Greek origin maps to the CRD locus for autosomal dominant cone-rod dystrophy on 19q'. Journal of Medical Genetics, 35 (5). pp. 429 - 431. ISSN: 0022-2593

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Bridger, JM. and Bickmore, WA. (1998) 'Putting the genome on the map'. Trends in Genetics, 14 (10). pp. 403 - 409. ISSN: 0168-9525 Open Access Link

Bessant, DAR., Payne, AM., Plant, C., Bird, AC. and Bhattacharya, SS. (1998) 'Further refinement of the Usher 2A locus at 1q41'. Journal of Medical Genetics, 35 (9). pp. 773 - 774. ISSN: 0022-2593

Bessant, DAR., Khaliq, S., Hameed, A., Anwar, K., Mehdi, SQ., Payne, AM. and Bhattacharya, SS. et al. (1998) 'A locus for autosomal recessive congenital microphthalmia maps to chromosome 14q32'. American Journal of Human Genetics, 62 (5). pp. 1113 - 1116. ISSN: 0002-9297

Roberts, T., Chernova, O. and Cowell, JK. (1998) 'Molecular characterization of the 1p22 breakpoint region spanning the constitutional translocation breakpoint in a neuroblastoma patient with a t(1;10)(p22;q21)'. Cancer Genetics and Cytogenetics, 100 (1). pp. 10 - 20. ISSN: 0165-4608

Payne, AM., Downes, SM., Bessant, DAR., Bird, AC. and Bhattacharya, SS. (1998) 'Founder effect, seen in the British population, of the 172 peripherin/RDS mutation- and further refinement of genetic positioning of the peripherin/RDS gene [2]'. American Journal of Human Genetics, 62 (1). pp. 192 - 195. ISSN: 0002-9297

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Weber, RG., Bridger, JM., Benner, A., Weisenberger, D., Ehemann, V., Reifenberger, G. and Lichter, P. et al. (1998) 'Centrosome amplification as a possible mechanism for numerical chromosome aberrations in cerebral primitive neuroectodermal tumors with TP53 mutations'. Cytogenet Cell Genetics, 83 (3-4). pp. 266 - 269. ISSN: 0301-0171 Open Access Link

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Forbes, SJ., Themis, M., Alison, MR., Selden, C., Coutelle, C. and Hodgson, HJF. (1998) 'Retroviral gene transfer to the liver in vivo during tri-iodothyronine induced hyperplasia'. Gene Therapy, 5 (4). pp. 552 - 555. ISSN: 0969-7128

Slijepcevic, P., Hande, MP., Bouffler, SD., Lansdorp, P. and Bryant, PE. (1997) 'Telomere length, chromatin structure and chromosome fusigenic potential'. Chromosoma, 106 (7). pp. 413 - 421. ISSN: 0009-5915

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Payne, AM., Downes, SM., Bessant, DAR., Taylor, R., Fitzke, FW., Holder, G., Bird, AC. and Bhattacharya, S. et al. (1997) 'New locus for autosomal dominant cone dystrophy mapping to 6p21.1.'. CELL PRESS. pp. A290 - A290. ISSN: 0002-9297

Wilmen, A., Strowski, M., Hofken, T., Fuller, P., Printz, H., Goke, B. and Wagner, ACC. et al. (1997) 'Differential display analysis reveals differential regulation of pancreatic genes during experimental pancreatitis'. GUT. pp. A75 - A75. ISSN: 0017-5749

Douar, AM., Adebakin, S., Themis, M., Pavirani, A., Cook, T. and Coutelle, C. (1997) 'Foetal gene delivery in mice by intra-amniotic administration of retroviral producer cells and adenovirus'. Gene Therapy, 4 (9). pp. 883 - 890. ISSN: 0969-7128

Still, IH., Roberts, T. and Cowell, JK. (1997) 'Fine structure physical mapping of a 1 center dot 9 Mb region of chromosome 13q12 (vol 61, pg 15, 1997)'. ANNALS OF HUMAN GENETICS, 61. pp. 379 - 379. ISSN: 0003-4800

Slijepcevic, P., Xiao, Y., Natarajan, AT. and Bryant, PE. (1997) 'Instability of cho chromosomes containing interstitial telomeric sequences originating fromchinese hamster chromosome 10'. Cytogenetics and Cell Genetics, 76 (1-2). pp. 58 - 60. ISSN: 0301-0171

Slijepcevic, P. and Bryant, PE. (1997) 'Telomere-mediated chromosome healing.'. Radiation research, 148 (3). pp. 293. ISSN: 0033-7587

Tosi, S., Mosna, G., Cazzaniga, G., Giudici, G., Kearney, L., Biondi, A. and Privitera, E. et al. (1997) 'Unbalanced t(3;12) in a case of juvenile myelomonocytic leukemia (JMML) results in partial trisomy of 3q as defined by FISH'. Leukemia, 11 (9). pp. 1465 - 1468. ISSN: 0887-6924