Larsson C - Search Results

1

Selective loss of chromosome 11 in pheochromocytomas associated with the VHL syndrome.

Lui WO, Chen J, Gläsker S, Bender BU, Madura C, Khoo SK, Kort E, Larsson C, Neumann HP, Teh BT. Lui WO, et al. Among authors: larsson c. Oncogene. 2002 Feb 7;21(7):1117-22. doi: 10.1038/sj.onc.1205149. Oncogene. 2002. PMID: 11850829

2

Predictive testing for multiple endocrine neoplasia type 1 using DNA polymorphisms.

Larsson C, Shepherd J, Nakamura Y, Blomberg C, Weber G, Werelius B, Hayward N, Teh B, Tokino T, Seizinger B. Larsson C, et al. J Clin Invest. 1992 Apr;89(4):1344-9. doi: 10.1172/JCI115720. J Clin Invest. 1992. PMID: 1348254 Free PMC article.

3

Morphology, DNA ploidy and allele losses on chromosome 11 in sporadic hyperparathyroidism and that associated with multiple neoplasia, type 1.

Sandelin K, Larsson C, Falkmer UG, Farnebo LO, Grimelius L, Nordenskjöld M. Sandelin K, et al. Among authors: larsson c. Eur J Surg. 1992 Apr;158(4):199-206. Eur J Surg. 1992. PMID: 1352132

4

Genomic alterations in human breast carcinomas.

Larsson C, Byström C, Skoog L, Rotstein S, Nordenskjöld M. Larsson C, et al. Genes Chromosomes Cancer. 1990 Sep;2(3):191-7. doi: 10.1002/gcc.2870020305. Genes Chromosomes Cancer. 1990. PMID: 1964080

5

Localization of the MEN1 gene to a small region within chromosome 11q13 by deletion mapping in tumors.

Byström C, Larsson C, Blomberg C, Sandelin K, Falkmer U, Skogseid B, Oberg K, Werner S, Nordenskjöld M. Byström C, et al. Among authors: larsson c. Proc Natl Acad Sci U S A. 1990 Mar;87(5):1968-72. doi: 10.1073/pnas.87.5.1968. Proc Natl Acad Sci U S A. 1990. PMID: 1968641 Free PMC article.

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. Among authors: larsson c. 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

Molecular tools for presymptomatic testing in multiple endocrine neoplasia type 1.

Larsson C, Calender A, Grimmond S, Giraud S, Hayward NK, Teh B, Farnebo F. Larsson C, et al. J Intern Med. 1995 Sep;238(3):239-44. doi: 10.1111/j.1365-2796.1995.tb00929.x. J Intern Med. 1995. PMID: 7673853

8

Candidate genes for multiple endocrine neoplasia type 1.

Lagercrantz J, Larsson C, Grimmond S, Skogseid B, Gobl A, Friedman E, Carson E, Phelan C, Oberg K, Nordenskjöld M, et al. Lagercrantz J, et al. Among authors: larsson c. J Intern Med. 1995 Sep;238(3):245-8. doi: 10.1111/j.1365-2796.1995.tb00930.x. J Intern Med. 1995. PMID: 7673854

9

Genetic mapping of the multiple endocrine neoplasia type 1 locus at 11q13.

Teh BT, Cardinal J, Shepherd J, Hayward NK, Weber G, Cameron D, Larsson C. Teh BT, et al. Among authors: larsson c. J Intern Med. 1995 Sep;238(3):249-53. doi: 10.1111/j.1365-2796.1995.tb00931.x. J Intern Med. 1995. PMID: 7673855

10

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. Among authors: larsson c. Am J Hum Genet. 1995 Jun;56(6):1443-9. Am J Hum Genet. 1995. PMID: 7762567 Free PMC article.

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