Teh BT - Search Results

1

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy.

Sullivan AA, Teh BT, Jeavons S, Schalling M, Silburn P, Larsson C, Boyle R. Sullivan AA, et al. Among authors: teh bt. J Clin Neurosci. 1997 Apr;4(2):176-80. doi: 10.1016/s0967-5868(97)90070-9. J Clin Neurosci. 1997. PMID: 18638952

2

Charcot-Marie-Tooth disease and Noonan syndrome with giant proximal nerve hypertrophy.

Silburn PA, Nicholson GA, Teh BT, Blair IP, Pollard JD, Nolan PJ, Larsson C, Boyle RS. Silburn PA, et al. Among authors: teh bt. Neurology. 1998 Apr;50(4):1067-73. doi: 10.1212/wnl.50.4.1067. Neurology. 1998. PMID: 9566396

3

Familial periodic cerebellar ataxia without myokymia maps to a 19-cM region on 19p13.

Teh BT, Silburn P, Lindblad K, Betz R, Boyle R, Schalling M, Larsson C. Teh BT, et al. Am J Hum Genet. 1995 Jun;56(6):1443-9. Am J Hum Genet. 1995. PMID: 7762567 Free PMC article.

4

Oculopharyngeal muscular dystrophy (OPMD)--report and genetic studies of an Australian kindred.

Teh BT, Sullivan AA, Farnebo F, Zander C, Li FY, Strachan N, Schalling M, Larsson C, Sandstrom P. Teh BT, et al. Clin Genet. 1997 Jan;51(1):52-5. doi: 10.1111/j.1399-0004.1997.tb02415.x. Clin Genet. 1997. PMID: 9084936

5

Bilateral multiple renal oncocytomas and cysts associated with a constitutional translocation (8;9)(q24.1;q34.3) and a rare constitutional VHL missense substitution.

Teh BT, Blennow E, Giraud S, Sahlén S, Hii SI, Brookwell R, Brauch H, Nordenskjöld M, Larsson C, Nicol D. Teh BT, et al. Genes Chromosomes Cancer. 1998 Mar;21(3):260-4. doi: 10.1002/(sici)1098-2264(199803)21:3<260::aid-gcc12>3.0.co;2-t. Genes Chromosomes Cancer. 1998. PMID: 9523203

6

Multiple endocrine neoplasia type I: clinical syndrome to molecular genetics.

Teh BT, Grimmond S, Shepherd J, Larsson C, Hayward N. Teh BT, et al. Aust N Z J Surg. 1995 Oct;65(10):708-13. doi: 10.1111/j.1445-2197.1995.tb00541.x. Aust N Z J Surg. 1995. PMID: 7487708 Review. No abstract available.

7

Gene identification in autosomal dominant disorders.

Teh BT, Lagercrantz J, Weber G, Larsson C. Teh BT, et al. AJNR Am J Neuroradiol. 1997 May;18(5):991-2. AJNR Am J Neuroradiol. 1997. PMID: 9159384 Free PMC article. No abstract available.

8

Exclusion of the 13-kDa rapamycin binding protein gene (FKBP2) as a candidate gene for multiple endocrine neoplasia type 1.

Grimmond S, Weber G, Larsson C, Walters M, Teh B, Shepherd J, Nordenskjold M, Hayward N. Grimmond S, et al. Hum Genet. 1995 Apr;95(4):455-8. doi: 10.1007/BF00208976. Hum Genet. 1995. PMID: 7535744

9

Characterization of the mouse Men1 gene and its expression during development.

Stewart C, Parente F, Piehl F, Farnebo F, Quincey D, Silins G, Bergman L, Carle GF, Lemmens I, Grimmond S, Xian CZ, Khodei S, Teh BT, Lagercrantz J, Siggers P, Calender A, Van de Vem V, Kas K, Weber G, Hayward N, Gaudray P, Larsson C. Stewart C, et al. Among authors: teh bt. Oncogene. 1998 Nov 12;17(19):2485-93. doi: 10.1038/sj.onc.1202164. Oncogene. 1998. PMID: 9824159

10

Sporadic primary hyperparathyroidism in the setting of multiple endocrine neoplasia type 1.

Teh BT, McArdle J, Parameswaran V, David R, Larsson C, Shepherd J. Teh BT, et al. Arch Surg. 1996 Nov;131(11):1230-2. doi: 10.1001/archsurg.1996.01430230112020. Arch Surg. 1996. PMID: 8911266

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