By Sverre Heim, Felix Mitelman
The 1st 3 variations of this acclaimed publication offered a much-needed conceptual synthesis of this quickly relocating box. Now, Cancer Cytogenetics, Fourth variation, bargains a finished, accelerated, and up to date evaluation of modern dramatic advances during this region, incorporating an enormous volume of recent facts from the most recent easy and scientific investigations.
- New members reflecting broader overseas authorship or even better expertise
- Greater emphasis all through at the scientific significance and alertness of data approximately cytogenetic and molecular aberrations
- Includes an entire assurance of chromosome aberrations in melanoma in line with an evaluation of the 60,000 neoplasms cytogenetically investigated to date
- Now produced in complete colour for greater clarity
- Covers how molecular genetic information (PCR-based and sequencing details) are collated with the cytogenetic info the place pertinent
- Discusses how molecular cytogenetic info (based on stories utilizing FISH, CGH, SNP, and so on) are fused with karyotyping info to allow an as complete knowing of melanoma cytogenetics as is presently possible
Read Online or Download Cancer Cytogenetics: Chromosomal and Molecular Genetic Aberrations of Tumor Cells PDF
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Extra resources for Cancer Cytogenetics: Chromosomal and Molecular Genetic Aberrations of Tumor Cells
The autosomes are numbered from 1 to 22 in descending order of length; the sex chromosomes are referred to as X and Y. 1. Designation of regions and bands Each chromosome arm—the short arm is called p, the long one q—may consist of one or more regions. Each region is delimited by specific landmarks, that is, consistent, distinct, morphologic features of impor tance in chromosome identification. Landmarks include the ends of chromosome arms (the telo meres), the centromere, and also certain characteristic bands.
For example, ins(5;2) (p14;q22q32) means that breakage and reunion have occurred at band 5p14 in the short arm of chromosome 5 and bands 2q22 and 2q32 in the long arm of chromosome 2. The segment from 2q22 to 2q32 has been inserted into 5p at band 5p14. The designation ins(2)(q13p13p23) describes an inser tion of the segment between bands 2p13 and 2p23 into the long arm of chromosome 2 at 2q13. Inversion, abbreviated inv: This designates a rotation 180° of a chromosome segment. In the karyotype 46,XY,inv(16)(p13q22), breakage and reunion have occurred at bands 16p13 and 16q22.
In contrast, del(1)(q21q31) indicates an interstitial deletion with breakage and reunion at bands 1q21 and 1q31. 5). The breakpoints delineate the dupli cated segment, for example, dup(1)(q21q31). Isochromosome, abbreviated i: Isochromosomes consist of arms that are mirror images of one another. They result from misdivision of the cen tromere (transverse breakage). 6). The designation i(12p) may be used in text, but the isochromosome should be written as i(12)(p10) in karyotype descriptions. The “band” 12p10 is a fictitious one; it is the side of the midcentromeric plane that faces toward the short arm.