Pejovic T - Search Results

1

Consistent occurrence of a 19p+ marker chromosome and loss of 11p material in ovarian seropapillary cystadenocarcinomas.

Pejovic T, Heim S, Mandahl N, Elmfors B, Flodérus UM, Furgyik S, Helm G, Willén H, Mitelman F. Pejovic T, et al. Genes Chromosomes Cancer. 1989 Nov;1(2):167-71. doi: 10.1002/gcc.2870010210. Genes Chromosomes Cancer. 1989. PMID: 2487157

2

Chromosome aberrations in 35 primary ovarian carcinomas.

Pejovic T, Heim S, Mandahl N, Baldetorp B, Elmfors B, Flodérus UM, Furgyik S, Helm G, Himmelmann A, Willén H, et al. Pejovic T, et al. Genes Chromosomes Cancer. 1992 Jan;4(1):58-68. doi: 10.1002/gcc.2870040108. Genes Chromosomes Cancer. 1992. PMID: 1377010

3

Prognostic impact of chromosome aberrations in ovarian cancer.

Pejovic T, Himmelmann A, Heim S, Mandahl N, Flodérus UM, Furgyik S, Elmfors B, Helm G, Willén H, Mitelman F. Pejovic T, et al. Br J Cancer. 1992 Feb;65(2):282-6. doi: 10.1038/bjc.1992.56. Br J Cancer. 1992. PMID: 1739630 Free PMC article.

4

Bilateral ovarian carcinoma: cytogenetic evidence of unicentric origin.

Pejovic T, Heim S, Mandahl N, Elmfors B, Furgyik S, Flodérus UM, Helm G, Willén H, Mitelman F. Pejovic T, et al. Int J Cancer. 1991 Feb 1;47(3):358-61. doi: 10.1002/ijc.2910470308. Int J Cancer. 1991. PMID: 1993543

5

Trisomy 12 is a consistent chromosomal aberration in benign ovarian tumors.

Pejovic T, Heim S, Mandahl N, Elmfors B, Flodérus UM, Furgyik S, Helm G, Willén H, Mitelman F. Pejovic T, et al. Genes Chromosomes Cancer. 1990 May;2(1):48-52. doi: 10.1002/gcc.2870020109. Genes Chromosomes Cancer. 1990. PMID: 2177641

6

Complex karyotypic anomalies, including an i(5p) marker chromosome, in malignant mixed mesodermal tumor of the ovary.

Pejovic T, Heim S, Mandahl N, Flodérus UM, Willén H, Mitelman F. Pejovic T, et al. Cancer Genet Cytogenet. 1990 May;46(1):65-9. doi: 10.1016/0165-4608(90)90009-y. Cancer Genet Cytogenet. 1990. PMID: 2331684

7

Simple numerical chromosome aberrations in well-differentiated malignant epithelial tumors.

Pejovic T, Heim S, Orndal C, Jin YS, Mandahl N, Willén H, Mitelman F. Pejovic T, et al. Cancer Genet Cytogenet. 1990 Oct 1;49(1):95-101. doi: 10.1016/0165-4608(90)90168-a. Cancer Genet Cytogenet. 1990. PMID: 2397477

8

Mapping of the 19p13 breakpoint in an ovarian carcinoma between the INSR and TCF3 loci.

Aman P, Pejovic T, Wennborg A, Heim S, Mitelman F. Aman P, et al. Among authors: pejovic t. Genes Chromosomes Cancer. 1993 Oct;8(2):134-6. doi: 10.1002/gcc.2870080212. Genes Chromosomes Cancer. 1993. PMID: 7504518

9

Isochromosome 1q as the sole karyotypic abnormality in a Sertoli cell tumor of the ovary.

Pejovic T, Heim S, Alm P, Iosif S, Himmelmann A, Skjaerris J, Mitelman F. Pejovic T, et al. Cancer Genet Cytogenet. 1993 Jan;65(1):79-80. doi: 10.1016/0165-4608(93)90065-t. Cancer Genet Cytogenet. 1993. PMID: 8431922

10

Cytogenetic findings in four malignant mixed mesodermal tumors of the ovary.

Pejovic T, Alm P, Iosif SC, Mitelman F, Heim S. Pejovic T, et al. Cancer Genet Cytogenet. 1996 May;88(1):53-6. doi: 10.1016/0165-4608(95)00291-x. Cancer Genet Cytogenet. 1996. PMID: 8630980

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