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Results 1 - 10 of 24 for Partial duplication of chromosome 3
  1. ... long arm of the chromosome in each cell (partial monosomy 16q).For example, ... syndrome, which is characterized by intellectual disability, distinctive ...
  2. ... M, Tiziano F, Di Stefano C, Neri G. Partial duplication of the long arm of chromosome 15: confirmation of a causative role in craniosynostosis ...
  3. ... Qumsiyeh MB, Tharapel AT, Summitt JB, Wilroy RS. Partial duplication of the long arm of chromosome 6: a clinically recognisable syndrome. J Med Genet. ...
  4. ... the duplicated segments can range in size from 3.2 Mb to 19.7 Mb. These duplications affect one of the two copies of chromosome 17 in each cell.The duplications that cause ...
  5. ... syndrome. More About This Health Condition 22q11.2 duplication is caused by an extra copy of some genetic material at position q11.2 on chromosome 22. In most cases, this extra genetic material consists of a sequence of about 3 million base pairs, also written as 3 megabases ( ...
  6. ... PubMed Lemire EG, Cardwell S. Unusual phenotype in partial trisomy 14. Am J Med Genet. 1999 Dec 3;87(4):294-6. doi: 10.1002/(sici) ...
  7. ... of the long (q) arm. The deletion and duplication result in the recombinant 8 chromosome. On the recombinant 8 chromosome, there is one copy of each of the genes instead of the usual two on the section of chromosome 8p that is deleted; and there are three copies each of the genes on the section ...
  8. ... is under study. More About This Health Condition ... segment ranges in size from about 3 Mb to nearly 20 Mb and always contains ...
  9. Talking Glossary of Genetic Terms From the National Institutes of Health (National Human Genome Research Institute)  
    Genetic Counseling/Reference Desk ... Genetic Counseling ... Genetic Testing/Reference Desk ... Genetic Testing ... Birth Defects/Reference Desk ... Birth Defects ... Genes and Gene ...
  10. ... 20 syndrome. Acta Neurol Scand. 2005 Mar;111(3):205-8. doi: 10.1111/j.1600-0404.2005.00298.x. Citation on PubMed Oppenheimer S, Dignan P, Soukup S. Partial trisomy 20p: familial occurrence. Am J Med Genet. ...
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