Wong FK - Search Results

1

Association of a novel constitutional translocation t(1q;3q) with familial renal cell carcinoma.

Kanayama H, Lui WO, Takahashi M, Naroda T, Kedra D, Wong FK, Kuroki Y, Nakahori Y, Larsson C, Kagawa S, Teh BT. Kanayama H, et al. Among authors: wong fk. J Med Genet. 2001 Mar;38(3):165-70. doi: 10.1136/jmg.38.3.165. J Med Genet. 2001. PMID: 11238683 Free PMC article.

2

Founder effect in multiple endocrine neoplasia type 1 (MEN 1) in Finland.

Kytölä S, Villablanca A, Ebeling T, Nord B, Larsson C, Höög A, Wong FK, Välimäki M, Vierimaa O, Teh BT, Salmela PI, Leisti J. Kytölä S, et al. Among authors: wong fk. J Med Genet. 2001 Mar;38(3):185-9. doi: 10.1136/jmg.38.3.185. J Med Genet. 2001. PMID: 11303512 Free PMC article. No abstract available.

3

Genetic heterogeneity and exclusion of a modifying locus at 17p11.2-p11.1 in Finnish families with van der Woude syndrome.

Wong FK, Koillinen H, Rautio J, Teh BT, Ranta R, Karsten A, Larson O, Linder-Aronson S, Huggare J, Larsson C, Kere J. Wong FK, et al. J Med Genet. 2001 Mar;38(3):198-202. doi: 10.1136/jmg.38.3.198. J Med Genet. 2001. PMID: 11303516 Free PMC article. No abstract available.

4

Sporadic follicular thyroid tumors show loss of a 200-kb region in 11q13 without evidence for mutations in the MEN1 gene.

Nord B, Larsson C, Wong FK, Wallin G, Teh BT, Zedenius J. Nord B, et al. Among authors: wong fk. Genes Chromosomes Cancer. 1999 Sep;26(1):35-9. doi: 10.1002/(sici)1098-2264(199909)26:1<35::aid-gcc5>3.0.co;2-l. Genes Chromosomes Cancer. 1999. PMID: 10441003

5

Familial isolated hyperparathyroidism maps to the hyperparathyroidism-jaw tumor locus in 1q21-q32 in a subset of families.

Teh BT, Farnebo F, Twigg S, Höög A, Kytölä S, Korpi-Hyövälti E, Wong FK, Nordenström J, Grimelius L, Sandelin K, Robinson B, Farnebo LO, Larsson C. Teh BT, et al. Among authors: wong fk. J Clin Endocrinol Metab. 1998 Jun;83(6):2114-20. doi: 10.1210/jcem.83.6.4896. J Clin Endocrinol Metab. 1998. PMID: 9626148

6

Clinical and genetic studies of Van der Woude syndrome in Sweden.

Wong FK, Karsten A, Larson O, Huggare J, Hagberg C, Larsson C, Teh BT, Linder-Aronson S. Wong FK, et al. Acta Odontol Scand. 1999 Apr;57(2):72-6. doi: 10.1080/000163599428931. Acta Odontol Scand. 1999. PMID: 10445358

7

Alternative genetic pathways in parathyroid tumorigenesis.

Farnebo F, Kytölä S, Teh BT, Dwight T, Wong FK, Höög A, Elvius M, Wassif WS, Thompson NW, Farnebo LO, Sandelin K, Larsson C. Farnebo F, et al. Among authors: wong fk. J Clin Endocrinol Metab. 1999 Oct;84(10):3775-80. doi: 10.1210/jcem.84.10.6057. J Clin Endocrinol Metab. 1999. PMID: 10523029

8

A genotypic and histopathological study of a large Dutch kindred with hyperparathyroidism-jaw tumor syndrome.

Haven CJ, Wong FK, van Dam EW, van der Juijt R, van Asperen C, Jansen J, Rosenberg C, de Wit M, Roijers J, Hoppener J, Lips CJ, Larsson C, Teh BT, Morreau H. Haven CJ, et al. Among authors: wong fk. J Clin Endocrinol Metab. 2000 Apr;85(4):1449-54. doi: 10.1210/jcem.85.4.6518. J Clin Endocrinol Metab. 2000. PMID: 10770180

9

Loss of heterozygosity in sporadic parathyroid tumours: involvement of chromosome 1 and the MEN1 gene locus in 11q13.

Dwight T, Twigg S, Delbridge L, Wong FK, Farnebo F, Richardson AL, Nelson A, Zedenius J, Philips J, Larsson C, Teh BT, Robinson B. Dwight T, et al. Among authors: wong fk. Clin Endocrinol (Oxf). 2000 Jul;53(1):85-92. doi: 10.1046/j.1365-2265.2000.01010.x. Clin Endocrinol (Oxf). 2000. PMID: 10931084

10

Birt-Hogg-Dubé syndrome: mapping of a novel hereditary neoplasia gene to chromosome 17p12-q11.2.

Khoo SK, Bradley M, Wong FK, Hedblad MA, Nordenskjöld M, Teh BT. Khoo SK, et al. Among authors: wong fk. Oncogene. 2001 Aug 23;20(37):5239-42. doi: 10.1038/sj.onc.1204703. Oncogene. 2001. PMID: 11526515

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