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Results: 1-16 |
Results: 16
Computerization of clinical practice in Hong Kong
Authors: Leung, GM Johnston, JM Ho, LM Wong, FK Cameo, SC
Citation: Gm. Leung et al., Computerization of clinical practice in Hong Kong, INT J MED I, 62(2-3), 2001, pp. 143-154
Mapping of the second locus for the Van der Woude syndrome to chromosome 1p34
Authors: Koillinen, H Wong, FK Rautio, J Ollikainen, V Karsten, A Larson, O Teh, BT Huggare, J Lahermo, P Larsson, C Kere, J
Citation: H. Koillinen et al., Mapping of the second locus for the Van der Woude syndrome to chromosome 1p34, EUR J HUM G, 9(10), 2001, pp. 747-752
Birt-Hogg-Dube syndrome: mapping of a novel hereditary neoplasia gene to chromosome 17p12-q11.2
Authors: Khoo, SK Bradley, M Wong, FK Hedblad, MA Nordenskjold, M Teh, BT
Citation: Sk. Khoo et al., Birt-Hogg-Dube syndrome: mapping of a novel hereditary neoplasia gene to chromosome 17p12-q11.2, ONCOGENE, 20(37), 2001, pp. 5239-5242
Identification of a new mutation in the alpha 4(IV) collagen gene in a family with autosomal dominant Alport syndrome and hypercholesterolaemia
Authors: Ciccarese, M Casu, D Wong, FK Faedda, R Arvidsson, S Tonolo, G Luthman, H Satta, A
Citation: M. Ciccarese et al., Identification of a new mutation in the alpha 4(IV) collagen gene in a family with autosomal dominant Alport syndrome and hypercholesterolaemia, NEPH DIAL T, 16(10), 2001, pp. 2008-2012
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
Genetic heterogeneity and exclusion of a modifying locus at 17p11.2-p11.1 in Finnish families with van der Woude syndrome
Authors: Wong, FK Koillinen, H Rautio, J Teh, BT Ranta, R Karsten, A Larson, O Linder-Aronson, S Huggare, J
Citation: Fk. Wong et al., Genetic heterogeneity and exclusion of a modifying locus at 17p11.2-p11.1 in Finnish families with van der Woude syndrome, J MED GENET, 38(3), 2001, pp. 198-202
Linkage analysis of candidate regions in Swedish nonsyndromic cleft lip with or without cleft palate families
Authors: Wong, FK Hagberg, C Karsten, A Larson, O Gustavsson, M Huggare, J Larsson, C Teh, BT Linder-Aronson, S
Citation: Fk. Wong et al., Linkage analysis of candidate regions in Swedish nonsyndromic cleft lip with or without cleft palate families, CLEF PAL-CR, 37(4), 2000, pp. 357-362
Multiple endocrine neoplasia type 1
Authors: Wong, FK Burgess, J Nordenskjold, M Larsson, C Teh, BT
Citation: Fk. Wong et al., Multiple endocrine neoplasia type 1, SEM CANC B, 10(4), 2000, pp. 299-312
Loss of heterozygosity in sporadic parathyroid tumours: involvement of chromosome 1 and the MEN1 gene locus in 11q13.
Authors: Dwight, T Twigg, S Delbridge, L Wong, FK Farnebo, F Richardson, AL Nelson, A Zedenius, J Philips, J Larsson, C Teh, BT Robinson, B
Citation: T. Dwight et al., Loss of heterozygosity in sporadic parathyroid tumours: involvement of chromosome 1 and the MEN1 gene locus in 11q13., CLIN ENDOCR, 53(1), 2000, pp. 85-92
A genotypic and histopathological study of a large Dutch kindred with hyperparathyroidism-jaw tumor syndrome
Authors: Haven, CJ Wong, FK van Dam, EWCM van der Luijt, R van Asperen, C Jansen, J Rosenberg, C de Wit, M Roijers, J Hoppener, J Lips, CJ Larsson, C Teh, BT Morreau, H
Citation: Cj. Haven et al., A genotypic and histopathological study of a large Dutch kindred with hyperparathyroidism-jaw tumor syndrome, J CLIN END, 85(4), 2000, pp. 1449-1454
Familial isolated hyperparathyroidism as a variant of multiple endocrine neoplasia type 1 in a large Danish pedigree
Authors: Kassem, M Kruse, TA Wong, FK Larsson, C Teh, BT
Citation: M. Kassem et al., Familial isolated hyperparathyroidism as a variant of multiple endocrine neoplasia type 1 in a large Danish pedigree, J CLIN END, 85(1), 2000, pp. 165-167
Popliteal pterygium syndrome in a Swedish family - clinical findings and genetic analysis with the van der Woude syndrome locus at lq32-q41
Authors: Wong, FK Gustafsson, B
Citation: Fk. Wong et B. Gustafsson, Popliteal pterygium syndrome in a Swedish family - clinical findings and genetic analysis with the van der Woude syndrome locus at lq32-q41, ACT ODON SC, 58(2), 2000, pp. 85-88
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
Alternative genetic pathways in parathyroid tumorigenesis
Authors: Farnebo, F Kytola, S Teh, BT Dwight, T Wong, FK Hoog, A Elvius, M Wassif, WS Thompson, NW Farnebo, LO Sandelin, K Larsson, C
Citation: F. Farnebo et al., Alternative genetic pathways in parathyroid tumorigenesis, J CLIN END, 84(10), 1999, pp. 3775-3780
Characterization of the MEN1 ortholog in zebrafish
Authors: Khodaei, S O'Brien, KP Dumanski, J Wong, FK Weber, G
Citation: S. Khodaei et al., Characterization of the MEN1 ortholog in zebrafish, BIOC BIOP R, 264(2), 1999, pp. 404-408
Clinical and genetic studies of Van der Woude syndrome in Sweden
Authors: Wong, FK Karsten, A Larson, O Huggare, J Hagberg, C Larsson, C Teh, BT Linder-Aronson, S
Citation: Fk. Wong et al., Clinical and genetic studies of Van der Woude syndrome in Sweden, ACT ODON SC, 57(2), 1999, pp. 72-76
Risultati: 1-16 |