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Partial deletion of the long arm of chromosome 16
- ... or 16q) and a missing segment of the long arm of the chromosome in each cell (partial monosomy 16q).For example, a region of DNA on chromosome 16 that includes the CREBBP gene is copied (duplicated) ...
- ... chromosome. Less commonly, the deletion occurs within the long arm of the chromosome, which is known as an interstitial deletion. The size of the deletion varies among affected individuals, with most affected people missing 5 million to 16 million DNA building blocks (base pairs). Larger deletions ...
- ... genetic material at the end (terminus) of the long (q) arm of chromosome 11. The size of the deletion varies among affected individuals, with most affected people missing about 5 million to 16 million DNA building blocks (base pairs). In almost ...
- ... long arm of the chromosome in each cell (partial monosomy 5q), and a circular ... Deletions in the long (q) arm of chromosome 5 frequently occur in ...
- ... MJ, Schmitt M, Jonveaux PH, LeHeup B. Terminal deletion of the long arm of ... in acute myeloid leukemia. Leukemia. 2002 Mar;16(3):344-51. doi: 10.1038/sj.leu. ...
- ... syndrome. 18q deletion syndrome 18q- syndrome Chromosome 18 long arm deletion syndrome Chromosome 18q deletion syndrome Chromosome 18q monosomy Chromosome 18q- ...
- ... Qumsiyeh MB, Tharapel AT, Summitt JB, Wilroy RS. Partial duplication of the long arm of chromosome 6: a clinically recognisable syndrome. J Med Genet. ...
- ... 1q), a missing segment of the short or long arm of the chromosome in each cell (partial monosomy 1p or 1q), or a circular structure called ring chromosome 1. Ring chromosomes occur when a chromosome breaks in two ... and conditions related to cancer. Deletions in the p arm of the chromosome have ...
- ... M, Tiziano F, Di Stefano C, Neri G. Partial duplication of the long arm of chromosome 15: confirmation of a causative role in craniosynostosis ...
- ... copy of chromosome 9 in each cell. The deletion occurs near the end of the long (q) arm of the chromosome at a location designated q34.3, a region containing a gene called EHMT1. Some affected individuals have shorter or longer deletions in the same region.The loss of the ...