Kiechle-Schwarz M - Search Results

1

Nonrandom cytogenetic changes in leiomyomas of the female genitourinary tract. A report of 35 cases.

Kiechle-Schwarz M, Sreekantaiah C, Berger CS, Pedron S, Medchill MT, Surti U, Sandberg AA. Kiechle-Schwarz M, et al. Cancer Genet Cytogenet. 1991 May;53(1):125-36. doi: 10.1016/0165-4608(91)90124-d. Cancer Genet Cytogenet. 1991. PMID: 2036633 Review.

2

Cluster of trisomy 12 to tumors of the female genitourinary tract.

Kiechle-Schwarz M, Pfleiderer A, Sreekantaiah C, Berger CS, Medchill MT, Sandberg AA. Kiechle-Schwarz M, et al. Cancer Genet Cytogenet. 1991 Jul 15;54(2):273-5. doi: 10.1016/0165-4608(91)90223-h. Cancer Genet Cytogenet. 1991. PMID: 1884365 No abstract available.

3

Rearrangement of band 10q22 in leiomyoma and leiomyosarcoma of the uterus.

Kiechle-Schwarz M, Berger CS, Surti U, Sandberg AA. Kiechle-Schwarz M, et al. Cancer Genet Cytogenet. 1990 Jul 1;47(1):95-100. doi: 10.1016/0165-4608(90)90268-f. Cancer Genet Cytogenet. 1990. PMID: 2357691

4

Detection of monosomy in interphase nuclei and identification of marker chromosomes using biotinylated alpha-satellite DNA probes.

Kiechle-Schwarz M, Decker HJ, Berger CS, Fiebig HH, Sandberg AA. Kiechle-Schwarz M, et al. Cancer Genet Cytogenet. 1991 Jan;51(1):23-33. doi: 10.1016/0165-4608(91)90004-e. Cancer Genet Cytogenet. 1991. PMID: 1845850

5

Cytogenetic analysis of an adenoid cystic carcinoma of the Bartholin's gland. A rare, semimalignant tumor of the female genitourinary tract.

Kiechle-Schwarz M, Kommoss F, Schmidt J, Lukovic L, Walz L, Bauknecht T, Pfleiderer A. Kiechle-Schwarz M, et al. Cancer Genet Cytogenet. 1992 Jul 1;61(1):26-30. doi: 10.1016/0165-4608(92)90365-f. Cancer Genet Cytogenet. 1992. PMID: 1322232

6

Recurrent cytogenetic aberrations in human ovarian carcinomas.

Kiechle-Schwarz M, Bauknecht T, Schmidt J, Walz L, Pfleiderer A. Kiechle-Schwarz M, et al. Cancer Detect Prev. 1995;19(3):234-43. Cancer Detect Prev. 1995. PMID: 7750111

7

Recurrent cytogenetic aberrations and loss of constitutional heterozygosity in ovarian carcinomas.

Kiechle-Schwarz M, Bauknecht T, Karck U, Kommoss F, du Bois A, Pfleiderer A. Kiechle-Schwarz M, et al. Gynecol Oncol. 1994 Nov;55(2):198-205. doi: 10.1006/gyno.1994.1277. Gynecol Oncol. 1994. PMID: 7959284

8

Cytogenetic and in situ DNA-hybridization studies in intracranial tumors of a patient with central neurofibromatosis.

Wullich B, Kiechle-Schwarz M, Mayfrank L, Schempp W. Wullich B, et al. Hum Genet. 1989 Apr;82(1):31-4. doi: 10.1007/BF00288267. Hum Genet. 1989. PMID: 2714777

9

Cytogenetic studies on three pheochromocytomas derived from patients with von Hippel-Lindau syndrome.

Kiechle-Schwarz M, Neumann HP, Decker HJ, Dietrich C, Wullich B, Schempp W. Kiechle-Schwarz M, et al. Hum Genet. 1989 May;82(2):127-30. doi: 10.1007/BF00284043. Hum Genet. 1989. PMID: 2722187

10

Loss of constitutional heterozygosity on chromosome 11p in human ovarian cancer. Positive correlation with grade of differentiation.

Kiechle-Schwarz M, Bauknecht T, Wienker T, Walz L, Pfleiderer A. Kiechle-Schwarz M, et al. Cancer. 1993 Oct 15;72(8):2423-32. doi: 10.1002/1097-0142(19931015)72:8<2423::aid-cncr2820720821>3.0.co;2-p. Cancer. 1993. PMID: 8402459

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