Spycher M - Search Results

1

[Tumor diseases in families of 600 breast cancer patients with special reference to familial adenocarcinomatosis and the Li-Fraumeni-/SBLA syndrome].

Müller H, Mosimann S, Gebhardt M, Scott R, Spycher M, Weber W. Müller H, et al. Among authors: spycher m. Helv Chir Acta. 1992 May;59(1):239-45. Helv Chir Acta. 1992. PMID: 1526835 German.

2

[Hereditary p53 mutation in a patient with multiple tumors: significance for genetic counseling].

Scott RJ, Krummenacher F, Mary JL, Weber W, Spycher M, Müller H. Scott RJ, et al. Among authors: spycher m. Schweiz Med Wochenschr. 1993 Jun 26;123(25):1287-92. Schweiz Med Wochenschr. 1993. PMID: 8393584 German.

3

Breast cancer in first degree relatives of 180 female breast cancer patients.

Fürstenberger G, Christen H, Minder CE, Spycher M, Weber W. Fürstenberger G, et al. Among authors: spycher m. In Vivo. 1994 May-Jun;8(3):367-70. In Vivo. 1994. PMID: 7803720

4

BRCA1 mutations in a selected series of breast/ovarian cancer patients.

Garvin AM, Spycher M, Häner M, Torhorst J, Müller H, Herrmann R, Rochlitz C, Weber W, Scott RJ. Garvin AM, et al. Among authors: spycher m. J Med Genet. 1996 Sep;33(9):721-5. doi: 10.1136/jmg.33.9.721. J Med Genet. 1996. PMID: 8880569 Free PMC article.

5

Mutational analysis of the hMSH2 gene reveals a three base pair deletion in a family predisposed to colorectal cancer development.

Mary JL, Bishop T, Kolodner R, Lipford JR, Kane M, Weber W, Torhorst J, Müller H, Spycher M, Scott RJ. Mary JL, et al. Among authors: spycher m. Hum Mol Genet. 1994 Nov;3(11):2067-9. Hum Mol Genet. 1994. PMID: 7874129 No abstract available.

6

Novel germline APC gene mutation in a large familial adenomatous polyposis kindred displaying variable phenotypes.

Scott RJ, van der Luijt R, Spycher M, Mary JL, Müller A, Hoppeler T, Haner M, Müller H, Martinoli S, Brazzola PL, et al. Scott RJ, et al. Among authors: spycher m. Gut. 1995 May;36(5):731-6. doi: 10.1136/gut.36.5.731. Gut. 1995. PMID: 7797123 Free PMC article.

7

Mutational analysis of the first 14 exons of the adenomatous polyposis coli (APC) gene.

Dobbie Z, Spycher M, Hürliman R, Ammann R, Ammann T, Roth J, Müller A, Müller H, Scott RJ. Dobbie Z, et al. Among authors: spycher m. Eur J Cancer. 1994;30A(11):1709-13. doi: 10.1016/0959-8049(94)00294-f. Eur J Cancer. 1994. PMID: 7833149

8

Novel germline APC gene mutation in a large familial adenomatous polyposis kindred displaying variable phenotypes.

Scott RJ, van der Luijt R, Spycher M, Mary JL, Muller A, Hoppeler T, Haner M, Muller H, Martinoli S, Brazzola PL. Scott RJ, et al. Among authors: spycher m. Gut. 1996 May;38(5):794. Gut. 1996. PMID: 8707134 Free PMC article. No abstract available.

9

Correlation between the development of extracolonic manifestations in FAP patients and mutations beyond codon 1403 in the APC gene.

Dobbie Z, Spycher M, Mary JL, Häner M, Guldenschuh I, Hürliman R, Amman R, Roth J, Müller H, Scott RJ. Dobbie Z, et al. Among authors: spycher m. J Med Genet. 1996 Apr;33(4):274-80. doi: 10.1136/jmg.33.4.274. J Med Genet. 1996. PMID: 8730280 Free PMC article.

10

[Electron microscopy of the exocrine pancreas in experimental acute hypercalcemia].

Frick T, Spycher M, Kaiser A, Goodale RL, Largiadèr F. Frick T, et al. Among authors: spycher m. Helv Chir Acta. 1991 Feb;57(5):713-6. Helv Chir Acta. 1991. PMID: 1864739 German.

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