Wong FK - Search Results

1

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

2

Mapping of the second locus for the Van der Woude syndrome to chromosome 1p34.

Koillinen H, Wong FK, Rautio J, Ollikainen V, Karsten A, Larson O, Teh BT, Huggare J, Lahermo P, Larsson C, Kere J. Koillinen H, et al. Among authors: wong fk. Eur J Hum Genet. 2001 Oct;9(10):747-52. doi: 10.1038/sj.ejhg.5200713. Eur J Hum Genet. 2001. PMID: 11781685

3

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

4

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

5

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

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

Familial isolated hyperparathyroidism as a variant of multiple endocrine neoplasia type 1 in a large Danish pedigree.

Kassem M, Kruse TA, Wong FK, Larsson C, Teh BT. Kassem M, et al. Among authors: wong fk. J Clin Endocrinol Metab. 2000 Jan;85(1):165-7. doi: 10.1210/jcem.85.1.6299. J Clin Endocrinol Metab. 2000. PMID: 10634381 Clinical Trial.

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

Linkage analysis of candidate regions in Swedish nonsyndromic cleft lip with or without cleft palate families.

Wong FK, Hagberg C, Karsten A, Larson O, Gustavsson M, Huggare J, Larsson C, Teh BT, Linder-Aronson S. Wong FK, et al. Cleft Palate Craniofac J. 2000 Jul;37(4):357-62. doi: 10.1597/1545-1569_2000_037_0357_laocri_2.3.co_2. Cleft Palate Craniofac J. 2000. PMID: 10912714

10

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.

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