Larsson C - Search Results

1

Homozygotes for the autosomal dominant neoplasia syndrome (MEN1).

Brandi ML, Weber G, Svensson A, Falchetti A, Tonelli F, Castello R, Furlani L, Scappaticci S, Fraccaro M, Larsson C. Brandi ML, et al. Among authors: larsson c. Am J Hum Genet. 1993 Dec;53(6):1167-72. Am J Hum Genet. 1993. PMID: 7902670 Free PMC article.

2

Isolation and mapping of polymorphic cosmid clones used for sublocalization of the multiple endocrine neoplasia type 1 (MEN1) locus.

Larsson C, Weber G, Kvanta E, Lewis K, Janson M, Jones C, Glaser T, Evans G, Nordenskjöld M. Larsson C, et al. Hum Genet. 1992 May;89(2):187-93. doi: 10.1007/BF00217121. Hum Genet. 1992. PMID: 1350263

3

Sublocalization of the multiple endocrine neoplasia type 1 gene.

Larsson C, Weber G, Janson M. Larsson C, et al. Henry Ford Hosp Med J. 1992;40(3-4):159-61. Henry Ford Hosp Med J. 1992. PMID: 1362396 Free article.

4

Exclusion of FAU as the multiple endocrine neoplasia type 1 (MEN1) gene.

Kas K, Weber G, Merregaert J, Michiels L, Sandelin K, Skogseid B, Thompson N, Nordenskjöld M, Larsson C, Friedman E. Kas K, et al. Among authors: larsson c. Hum Mol Genet. 1993 Apr;2(4):349-53. doi: 10.1093/hmg/2.4.349. Hum Mol Genet. 1993. PMID: 8099302

5

Exclusion of the phosphoinositide-specific phospholipase C beta 3 (PLCB3) gene as a candidate for multiple endocrine neoplasia type 1.

Weber G, Grimmond S, Lagercrantz J, Friedman E, Phelan C, Carson E, Hayward N, Jacobovitz O, Nordenskjöld M, Larsson C. Weber G, et al. Among authors: larsson c. Hum Genet. 1997 Jan;99(1):130-2. doi: 10.1007/s004390050326. Hum Genet. 1997. PMID: 9003510

6

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. Among authors: larsson c. Hum Genet. 1995 Apr;95(4):455-8. doi: 10.1007/BF00208976. Hum Genet. 1995. PMID: 7535744

7

Genetics of multiple endocrine neoplasia type 1.

Larsson C, Weber G, Teh BT, Lagercrantz J. Larsson C, et al. Ann N Y Acad Sci. 1994 Sep 15;733:453-63. doi: 10.1111/j.1749-6632.1994.tb17295.x. Ann N Y Acad Sci. 1994. PMID: 7978894 Review. No abstract available.

8

Mapping of the gene encoding the B56 beta subunit of protein phosphatase 2A (PPP2R5B) to a 0.5-Mb region of chromosome 11q13 and its exclusion as a candidate gene for multiple endocrine neoplasia type 1 (MEN1).

Forbes SA, Pannett AA, Bassett JH, Harding B, Wooding C, Thakker RV, Butler R, Ogilvie D, Anand R, Gaudray P, Weber G, Larsson C, Zhang CX, Calender A, Höppener JW, Lips CJ, Kas K. Forbes SA, et al. Among authors: larsson c. Hum Genet. 1997 Sep;100(3-4):481-5. doi: 10.1007/s004390050538. Hum Genet. 1997. PMID: 9272177

9

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.

10

Differential loss of heterozygosity in familial, sporadic, and uremic hyperparathyroidism.

Farnebo F, Teh BT, Dotzenrath C, Wassif WS, Svensson A, White I, Betz R, Goretzki P, Sandelin K, Farnebo LO, Larsson C. Farnebo F, et al. Among authors: larsson c. Hum Genet. 1997 Mar;99(3):342-9. doi: 10.1007/s004390050369. Hum Genet. 1997. PMID: 9050920

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