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Partial duplication of the long arm of chromosome 4
- ... M, Tiziano F, Di Stefano C, Neri G. Partial duplication of the long arm of chromosome 15: confirmation of a causative role in craniosynostosis and definition of a 15q25-qter trisomy syndrome. Am J Med Genet. 1999 Dec 22;87(5):391-4. doi: 10.1002/(sici)1096-8628(19991222)87: ...
- ... Qumsiyeh MB, Tharapel AT, Summitt JB, Wilroy RS. Partial duplication of the long arm of chromosome 6: a clinically recognisable syndrome. J Med Genet. ...
- ... building blocks (base pairs), also written as 1.4 megabases (Mb), on the long ... duplication (described below). This chromosome segment is surrounded by ...
- ... or 16q) and a missing segment of the long arm of the chromosome in each cell ... syndrome, which is characterized by intellectual disability, distinctive ...
- ... the growth and division of cells. ... of the chromosome in each cell (partial trisomy 20p or 20q) or a missing segment ...
- ... 5p or 5q), a missing segment of the long arm of the chromosome in each cell (partial monosomy 5q), and a circular structure called ring chromosome 5. Ring chromosomes occur when a chromosome breaks in two places and the ends ... Deletions in the long (q) arm of chromosome 5 frequently occur in ...
- ... 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 ...
- ... and a duplication of a piece of the long (q) arm. The deletion and duplication result in the recombinant 8 chromosome. On the recombinant 8 chromosome, there is one ...
- ... number of copies of chromosome 7. 7q11.23 duplication syndrome, a condition that can cause a variety of neurological and behavioral problems as well as other abnormalities, results from an extra copy of a region on the long (q) arm of chromosome 7. This region is called the Williams-Beuren ...
- ... other problems that affect some people with this duplication. More About This Health Condition 22q13.3 deletion syndrome, which is also commonly known as Phelan-McDermid syndrome, is caused by a deletion near the end of the long (q) arm of chromosome 22. A ring chromosome 22 can also cause ...