N	Concordance
1	astomas with cytogenetic abnormalities, chromosome 1 was most frequently affecte
2	 of trisomy 18 due to a pseudodicentric chromosome 18 of paternal origin. The ka
3	ative tumour suppressor gene located on chromosome 1p32-pter, a region that repr
4	he EGR-1 gene, shows synteny with human chromosome 5q, a region strongly associa
5	te the characteristics of the numerical chromosome aberrations in liver metastas
6	cluding two copies of the translocation chromosome and hence effectively trisomi
7	nding patterns as revealed by different chromosome banding techniques. Thus, chr
8	T4 and STAT1 genes were mapped to human chromosome bands 2q32.2-->q32.3 by fluor
9	normal sperm cells carrying an abnormal chromosome constitution (XX or YY or XY 
10	 up the chromosomes. An "average" sized chromosome contains enough DNA to accoun
11	notype correlates with a largely stable chromosome content during long-term cult
12	n addition, the alterations of specific chromosome copy number could be detected
13	al microscopy indicated that homologous chromosome domains were re-positioned cl
14	 cerevisiae that block meiotic prophase chromosome metabolism and confer cell cy
15	n age was 52 years; 36 had Philadelphia chromosome-positive disease. Decitabine 
16	C protein may play an important role in chromosome segregation during M phase.  
17	s pigmentosa region by yeast artificial chromosome (YAC) and establish the restr