Sentence examples for most frequent chromosomal from inspiring English sources

Deletion of chromosome 13q is the most frequent chromosomal aberration in CLL, occurring in approximately 50% of patients [2].

Deletion of chromosome 13q14 is the most frequent chromosomal abnormality in this disorder.

Deletion of chromosome 13q14 is the most frequent chromosomal abnormality in this disorder and it has been postulated that a tumour suppressor gene resides in this region.

Gain of chromosome arm 17q is the most frequent chromosomal change in neuroblastoma [13] suggesting that this region includes genes critical for tumorigenesis.

The most frequent chromosomal abnormality in neuroblastomas is gain of chromosome 17 [43], which appears to conflict with a potential tumor suppressor function for ACCN1 in neuroblastoma.

The most frequent chromosomal abnormalities are partial losses of one affected chromosome, such as deletions on 6q, 11q, 13q, or 17p; gains of entire chromosomes, such as trisomy 12, are less frequent.

In several candidate chromosomal regions with relevance for ASDs, duplication of human chromosome 15q11-13 is the most frequent chromosome rearrangement, found in 1 4% of ASDs patients [5].

CNVplex® uses 42 probes outside 22q11.2 according to the most-frequent chromosomal findings to optimize the diagnostic protocol [ 19].

Translocations of chromosomal band 2p21 are the second most frequent structural chromosomal rearrangement, representing a particular cytogenetic subgroup [ 2].

Del22q11.2 syndrome is the most frequent known chromosomal microdeletion syndrome.

One of the most frequent nonrandom chromosomal CNAs confirmed in ccRCC is 9p deletion [ 17– 20].