Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Catherine S. Rodgers"'
Autor:
David F. Callen, Catherine S. Rodgers, Robin M. Winter, Paul Cullen, Peter Fells, Rajesh V. Thakker, Vincent M. Connolly, Harold Gordon, Helen J. Eyre
Publikováno v:
American journal of medical genetics. 47(6)
We report a spectrum of defects that were found in an 18-year-old girl who presented for investigation of primary amenorrhea. The patient was found to have Duane anomaly, left renal agenesis, absent uterus, bilateral sensorineural deafness, and bilat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bbaca1d5a348e750c20d8fd33a25bd7f
https://pubmed.ncbi.nlm.nih.gov/8279492
https://pubmed.ncbi.nlm.nih.gov/8279492
Publikováno v:
Cancer Genetics and Cytogenetics. 15:113-117
Sequential chromosome banding of direct preparations from an infiltrating ductal carcinoma of the left breast of a male, aged 56 years, showed a diploid chromosome range with a mode at 44. Consistent monosomy of chromosomes #2, #3, #4, #6, #11, #15,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1c1817028bd10323b3adae8c27d06aa5
https://doi.org/10.1016/0165-4608(85)90138-4
https://doi.org/10.1016/0165-4608(85)90138-4
Autor:
Sally M. Hill, Maj A. Hultén, Catherine S. Rodgers, Sidney E. Chang, Jacqueline Keen, Joyce Taylor-Papadimitriou
Publikováno v:
Cancer Genetics and Cytogenetics. 8:213-221
The SV40-transformed breast epithelial cell lines established by Chang et al. [1] were shown to be hypotetraploid and characterized by six chromosome markers: M1 i(1q), M2 del(1)(q21), M3 i(6p), M4 del(1)(q11), M5 t(8p;12q), and M6 dir dup(11)(p12→
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8c8a7dae214cc5010ad54c5a2ee90fc4
https://doi.org/10.1016/0165-4608(83)90137-1
https://doi.org/10.1016/0165-4608(83)90137-1
Publikováno v:
Cancer genetics and cytogenetics. 24(1)
This report presents karyotypes of seven breast carcinomas with high ploidy from our total of 111 cases. These karyotypes were highly complex and there was no indication of a specific deletion of 16p12→pter as indicated by the previous analysis of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c1358ff280b00f766d0e1c00b5dde44e
https://pubmed.ncbi.nlm.nih.gov/3024810
https://pubmed.ncbi.nlm.nih.gov/3024810
Publikováno v:
Cancer genetics and cytogenetics. 12(4)
The cell line OAW 42 was established from the ascites of a patient with papillary serous cystadenocarcinoma of the ovary. Cytogenetic analysis at three different passages showed that the line was hypotetraploid, with no distinct mode, and was charact
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::84b9c943fb283cff96d27ef3da3b6221
https://pubmed.ncbi.nlm.nih.gov/6744227
https://pubmed.ncbi.nlm.nih.gov/6744227
Publikováno v:
Cancer genetics and cytogenetics. 13(2)
Cells in mitosis were found in 51 of 110 (47%) breast tumor samples; karyotypes of nine tumors in the diploid range are presented. The simplest stemline karyotype found was 46,XX,−16,+del(1)(qter→p21). The chromosome homologues most frequently lo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::47696da9d833d35fdb8142eb33a93e4b
https://pubmed.ncbi.nlm.nih.gov/6090007
https://pubmed.ncbi.nlm.nih.gov/6090007