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Results: 1-7 |
Results: 7
Founder effect in multiple endocrine neoplasia type 1 (MEN 1) in Finland
Authors: Kytola, S Villablanca, A Ebelings, T Nord, B Larsson, C Hoog, A Wong, FK Valimaki, M Vierimaa, O Teh, BT Salmela, PI Leisti, J
Citation: S. Kytola et al., Founder effect in multiple endocrine neoplasia type 1 (MEN 1) in Finland, J MED GENET, 38(3), 2001, pp. 185-189
Comparative genomic hybridization identifies loss of 18q22-qter as an early and specific event in tumorigenesis of midgut carcinoids
Authors: Kytola, S Hoog, A Nord, B Cedermark, B Frisk, T Larsson, C Kjellman, M
Citation: S. Kytola et al., Comparative genomic hybridization identifies loss of 18q22-qter as an early and specific event in tumorigenesis of midgut carcinoids, AM J PATH, 158(5), 2001, pp. 1803-1808
Phenotype and phenocopy: the relationship between genotype and clinical phenotype in a single large family with multiple endocrine neoplasia type 1 (MEN 1)
Authors: Burgess, JR Nord, B David, R Greenaway, TM Parameswaran, V Larsson, C Shepherd, JJ Teh, BT
Citation: Jr. Burgess et al., Phenotype and phenocopy: the relationship between genotype and clinical phenotype in a single large family with multiple endocrine neoplasia type 1 (MEN 1), CLIN ENDOCR, 53(2), 2000, pp. 205-211
Malignant melanoma in patients with multiple endocrine neoplasia type 1 and involvement of the MEN1 gene in sporadic melanoma
Authors: Nord, B Platz, A Smoczynski, K Kytola, S Robertson, G Calender, A Murat, A Weintraub, D Burgess, J Edwards, M Skogseid, B Owen, D Lassam, N Hogg, D Larsson, C Teh, BT
Citation: B. Nord et al., Malignant melanoma in patients with multiple endocrine neoplasia type 1 and involvement of the MEN1 gene in sporadic melanoma, INT J CANC, 87(4), 2000, pp. 463-467
Comparative genomic hybridization reveals frequent losses of chromosomes 1p and 3q in pheochromocytomas and abdominal paragangliomas, suggesting a common genetic etiology
Authors: Edstrom, E Mahlamaki, E Nord, B Kjellman, M Karhu, R Hoog, A Goncharov, N Teh, BT Backdahl, M Larsson, C
Citation: E. Edstrom et al., Comparative genomic hybridization reveals frequent losses of chromosomes 1p and 3q in pheochromocytomas and abdominal paragangliomas, suggesting a common genetic etiology, AM J PATH, 156(2), 2000, pp. 651-659
Sporadic follicular thyroid tumors show loss of a 200-kb region in 11q13 without evidence for mutations in the MEN1 gene
Authors: Nord, B Larsson, C Wong, FK Wallin, G Teh, BT Zedenius, J
Citation: B. Nord et al., Sporadic follicular thyroid tumors show loss of a 200-kb region in 11q13 without evidence for mutations in the MEN1 gene, GENE CHROM, 26(1), 1999, pp. 35-39
Familial testicular cancer: lack of evidence for trinucleotide repeat expansions and association with PKD1 in one family
Authors: Teh, BT Linblad, K Nord, B Kytola, S Schalling, M Larsson, C Rapley, E Biggs, P Huddart, R Stratton, M Hii, S Nicol, D
Citation: Bt. Teh et al., Familial testicular cancer: lack of evidence for trinucleotide repeat expansions and association with PKD1 in one family, J MED GENET, 36(4), 1999, pp. 348-349
Risultati: 1-7 |