Results: 1-13 |
Results: 13
Cribriform variant papillary thyroid cancer: A characteristic of familial adenomatous polyposis
Authors: Fenton, PA Clarke, SEM Owen, W Hibbert, J Hodgson, SV
Citation: Pa. Fenton et al., Cribriform variant papillary thyroid cancer: A characteristic of familial adenomatous polyposis, THYROID, 11(2), 2001, pp. 193-197
Hyperkalaemic cardiac arrest in a manifesting carrier of Duchenne musculardystrophy following general anaesthesia
Authors: Kerr, TP Durward, A Hodgson, SV Hughes, E Robb, SA
Citation: Tp. Kerr et al., Hyperkalaemic cardiac arrest in a manifesting carrier of Duchenne musculardystrophy following general anaesthesia, EUR J PED, 160(9), 2001, pp. 579-580
A mitotically stable marker chromosome negative for whole chromosome libraries, centromere probes and chromosome specific telomere regions: a novel class of supernumerary marker chromosome?
Authors: Ogilvie, CM Harrison, RH Horsley, SW Hodgson, SV Kearney, L
Citation: Cm. Ogilvie et al., A mitotically stable marker chromosome negative for whole chromosome libraries, centromere probes and chromosome specific telomere regions: a novel class of supernumerary marker chromosome?, CYTOG C GEN, 92(1-2), 2001, pp. 69-73
Cancer risks in women with 2 breast or ovarian cancers: Clues to genetic cancer susceptibility
Authors: Evans, HS Lewis, CM Robinson, D Bell, CMJ Moller, H Hodgson, SV
Citation: Hs. Evans et al., Cancer risks in women with 2 breast or ovarian cancers: Clues to genetic cancer susceptibility, INT J CANC, 94(5), 2001, pp. 758-759
Incidence of multiple primary cancers in a cohort of women diagnosed with breast cancer in southeast England
Authors: Evans, HS Lewis, CM Robinson, D Bell, CMJ Moller, H Hodgson, SV
Citation: Hs. Evans et al., Incidence of multiple primary cancers in a cohort of women diagnosed with breast cancer in southeast England, BR J CANC, 84(3), 2001, pp. 435-440
Germline mutations in BMPR1A/ALK3 cause a subset of cases of juvenile polyposis syndrome and of Cowden and Bannayan-Riley-Ruvalcaba syndromes
Authors: Zhou, XP Woodford-Richens, K Lehtonen, R Kurose, K Aldred, M Hampel, H Launonen, V Virta, S Pilarski, R Salovaara, R Bodmer, WF Conrad, BA Dunlop, M Hodgson, SV Iwama, T Jarvinen, H Kellokumpu, I Kim, JC Leggett, B Markie, D Mecklin, JP Neale, K Phillips, R Piris, J Rozen, P Houlston, RS Aaltonen, LA Tomlinson, IPM Eng, C
Citation: Xp. Zhou et al., Germline mutations in BMPR1A/ALK3 cause a subset of cases of juvenile polyposis syndrome and of Cowden and Bannayan-Riley-Ruvalcaba syndromes, AM J HU GEN, 69(4), 2001, pp. 704-711
Analysis of single-nucleotide polymorphisms in the interleukin-4 receptor gene for association with inflammatory bowel disease
Authors: Olavesen, MG Hampe, J Mirza, MM Saiz, R Lewis, CM Bridger, S Teare, D Easton, DF Herrmann, T Scott, G Hirst, J Sanderson, J Hodgson, SV Lee, J MacPherson, A Schreiber, S Lennard-Jones, JE Curran, ME Mathew, CG
Citation: Mg. Olavesen et al., Analysis of single-nucleotide polymorphisms in the interleukin-4 receptor gene for association with inflammatory bowel disease, IMMUNOGENET, 51(1), 2000, pp. 1-7
A survey of the current clinical facilities for the management of familialcancer in Europe
Authors: Hodgson, SV Haites, NE Caligo, M Chang-Claude, J Eccles, D Evans, G Moller, P Morrison, P Steel, CM Stoppa-Lyonnet, D Vasen, H
Citation: Sv. Hodgson et al., A survey of the current clinical facilities for the management of familialcancer in Europe, J MED GENET, 37(8), 2000, pp. 605-607
Analysis of genetic and phenotypic heterogeneity in juvenile polyposis
Authors: Woodford-Richens, K Bevan, S Churchman, M Dowling, B Jones, D Norbury, CG Hodgson, SV Desai, D Neale, K Phillips, RKS Young, J Leggett, B Dunlop, M Rozen, P Eng, C Markie, D Rodriguez-Bigas, MA Sheridan, E Iwama, T Eccles, D Smith, GT Kim, JC Kim, KM Sampson, JR Evans, G Tejpar, S Bodmer, WF Tomlinson, IPM Houlston, RS
Citation: K. Woodford-richens et al., Analysis of genetic and phenotypic heterogeneity in juvenile polyposis, GUT, 46(5), 2000, pp. 656-660
Rapid and efficient ATM mutation detection by fluorescent chemical cleavage of mismatch: identification of four novel mutations
Authors: Izatt, L Vessey, C Hodgson, SV Solomon, E
Citation: L. Izatt et al., Rapid and efficient ATM mutation detection by fluorescent chemical cleavage of mismatch: identification of four novel mutations, EUR J HUM G, 7(3), 1999, pp. 310-320
PTEN mutation spectrum and genotype-phenotype correlations in Bannayan-Riley-Ruvalcaba syndrome suggest a single entity with Cowden syndrome
Authors: Marsh, DJ Kum, JB Lunetta, KL Bennett, MJ Gorlin, RJ Ahmed, SF Bodurtha, J Crowe, C Curtis, MA Dasouki, M Dunn, T Feit, H Geraghty, MT Graham, JM Hodgson, SV Hunter, A Korf, BR Manchester, D Miesfeldt, S Murday, VA Nathanson, KL Parisi, M Pober, B Romano, C Tolmie, JL Trembath, R Winter, RM Zackai, EH Zori, RT Weng, LP Dahia, PLM Eng, C
Citation: Dj. Marsh et al., PTEN mutation spectrum and genotype-phenotype correlations in Bannayan-Riley-Ruvalcaba syndrome suggest a single entity with Cowden syndrome, HUM MOL GEN, 8(8), 1999, pp. 1461-1472
Cancer genetics services in the UK
Authors: Hodgson, SV
Citation: Sv. Hodgson, Cancer genetics services in the UK, DIS MARKER, 15(1-3), 1999, pp. 44-45
Risk factors for detecting germline BRCA1 and BRCA2 founder mutations in Ashkenazi Jewish women with breast or ovarian cancer
Authors: Hodgson, SV Heap, E Cameron, J Ellis, D Mathew, CG Eeles, RA Solomon, E Lewis, CM
Citation: Sv. Hodgson et al., Risk factors for detecting germline BRCA1 and BRCA2 founder mutations in Ashkenazi Jewish women with breast or ovarian cancer, J MED GENET, 36(5), 1999, pp. 369-373
Risultati: 1-13 |