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Results: 1-5 |
Results: 5
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
The small GTPase RAC3 gene is located within chromosome band 17q25.3 outside and telomeric of a region commonly deleted in breast and ovarian tumours
Authors: Morris, CM Haataja, L McDonald, M Gough, S Markie, D Groffen, J Heisterkamp, N
Citation: Cm. Morris et al., The small GTPase RAC3 gene is located within chromosome band 17q25.3 outside and telomeric of a region commonly deleted in breast and ovarian tumours, CYTOG C GEN, 89(1-2), 2000, pp. 18-23
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
Mutations and impaired function of LKB1 in familial and non-familial Peutz-Jeghers syndrome and a sporadic testicular cancer
Authors: Ylikorkala, A Avizienyte, E Tomlinson, IPM Tiainen, M Roth, S Loukola, A Hemminki, A Johansson, M Sistonen, P Markie, D Neale, K Phillips, R Zauber, P Twama, T Sampson, J Jarvinen, H Makela, TP Aaltonen, LA
Citation: A. Ylikorkala et al., Mutations and impaired function of LKB1 in familial and non-familial Peutz-Jeghers syndrome and a sporadic testicular cancer, HUM MOL GEN, 8(1), 1999, pp. 45-51
Screening SMAD1, SMAD2, SMAD3, and SMAD5 for germline mutations in juvenile polyposis syndrome
Authors: Bevan, S Woodford-Richens, K Rozen, P Eng, C Young, J Dunlop, M Neale, K Phillips, R Markie, D Rodriguez-Bigas, M Leggett, B Sheridan, E Hodgson, S Iwama, T Eccles, D Bodmer, W Houlston, R Tomlinson, I
Citation: S. Bevan et al., Screening SMAD1, SMAD2, SMAD3, and SMAD5 for germline mutations in juvenile polyposis syndrome, GUT, 45(3), 1999, pp. 406-408
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