POSSIBLY IDENTICAL MARKER CHROMOSOME DER(16)T(QUESTIONABLE 13-16)(QUESTIONABLE Q13OR14-Q22) IN A SQUAMOUS-CELL CARCINOMA OF THE SKIN AND LARYNX

被引：4

作者：

ATKIN, NB

FOX, MF

机构：

[1] Department of Cancer Research, Mount Vernon Hospital, Northwood, Middlesex

来源：

CANCER GENETICS AND CYTOGENETICS | 1992年 / 58卷 / 02期

关键词：

D O I：

10.1016/0165-4608(92)90113-M

中图分类号：

R73 [肿瘤学];

学科分类号：

100214 ;

摘要：

A possibly identical marker chromosome was seen in two squamous cell carcinomas, of the face and larynx respectively, in direct preparations or 24-hour cultures. The probable designation of the marker, which may represent a significant cytogenetic event contributing to the evolution of these tumors, was der(16)t(?13;16)(?q13or14;q22).

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页码：198 / 200

页数：3

相关论文

共 11 条

[1] CHROMOSOME CHANGES IN 43 CARCINOMAS OF THE CERVIX UTERI [J].

ATKIN, NB ;

BAKER, MC ;

FOX, MF .

CANCER GENETICS AND CYTOGENETICS, 1990, 44 (02) :229-241

[2]

ATKIN NB, 1988, CYTOBIOS, V54, P161

[3] SQUAMOUS-CELL CARCINOMAS OF THE HEAD, NECK, AND SKIN - MONOCLONAL OR POLYCLONAL ORIGIN [J].

ATKIN, NB ;

BAKER, MC .

CANCER GENETICS AND CYTOGENETICS, 1991, 54 (01) :135-136

[4]

DRYJA TP, 1986, AM J HUM GENET, V38, P59

[5] MULTIPLE UNRELATED CLONAL CHROMOSOME-ABNORMALITIES IN AN INSITU SQUAMOUS-CELL CARCINOMA OF THE SKIN [J].

HEIM, S ;

JIN, YS ;

MANDAHL, N ;

BIORKLUND, A ;

WENNERBERG, J ;

JONSSON, N ;

MITELMAN, F .

CANCER GENETICS AND CYTOGENETICS, 1988, 36 (02) :149-153

[6] DIVERSE CHROMOSOME-ABNORMALITIES IN SQUAMOUS-CELL CARCINOMAS OF THE SKIN [J].

HEIM, S ;

MERTENS, F ;

JIN, YS ;

MANDAHL, N ;

JOHANSSON, B ;

BIORKLUND, A ;

WENNERBERG, J ;

JONSSON, N ;

MITELMAN, F .

CANCER GENETICS AND CYTOGENETICS, 1989, 39 (01) :69-76

[7] MULTIPLE CLONAL CHROMOSOME-ABERRATIONS IN SQUAMOUS-CELL CARCINOMAS OF THE LARYNX [J].

JIN, YS ;

HEIM, S ;

MANDAHL, N ;

BIORKLUND, A ;

WENNERBERG, J ;

MITELMAN, F .

CANCER GENETICS AND CYTOGENETICS, 1990, 44 (02) :209-216

[8] LOSS OF HETEROZYGOSITY IN HUMAN DUCTAL BREAST-TUMORS INDICATES A RECESSIVE MUTATION ON CHROMOSOME-13 [J].

LUNDBERG, C ;

SKOOG, L ;

CAVENEE, WK ;

NORDENSKJOLD, M .

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (08) :2372-2376

[9]

MOTOMURA K, 1988, Genomics, V2, P180, DOI 10.1016/0888-7543(88)90101-2

[10] NO STATISTICAL ASSOCIATION BETWEEN COMMON FRAGILE SITES AND NONRANDOM CHROMOSOME BREAKPOINTS IN CANCER-CELLS [J].

SUTHERLAND, GR ;

SIMMERS, RN .

CANCER GENETICS AND CYTOGENETICS, 1988, 31 (01) :9-15