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Yang, C. 3p Deletion Syndrome. Encyclopedia. Available online: https://encyclopedia.pub/entry/4158 (accessed on 24 September 2026).
Yang C. 3p Deletion Syndrome. Encyclopedia. Available at: https://encyclopedia.pub/entry/4158. Accessed September 24, 2026.
Yang, Catherine. "3p Deletion Syndrome" Encyclopedia, https://encyclopedia.pub/entry/4158 (accessed September 24, 2026).
Yang, C. (2020, December 23). 3p Deletion Syndrome. In Encyclopedia. https://encyclopedia.pub/entry/4158
Yang, Catherine. "3p Deletion Syndrome." Encyclopedia. Web. 23 December, 2020.
3p Deletion Syndrome
Edit

3p deletion syndrome is a condition that results from a chromosomal change in which a small piece of chromosome 3 is deleted in each cell. The deletion occurs at the end of the short (p) arm of the chromosome. This chromosomal change often leads to intellectual disability, developmental delay, and abnormal physical features.

genetic conditions

References

  1. Kellogg G, Sum J, Wallerstein R. Deletion of 3p25.3 in a patient withintellectual disability and dysmorphic features with further definition of acritical region. Am J Med Genet A. 2013 Jun;161A(6):1405-8. doi:10.1002/ajmg.a.35876.
  2. Malmgren H, Sahlén S, Wide K, Lundvall M, Blennow E. Distal 3p deletionsyndrome: detailed molecular cytogenetic and clinical characterization of threesmall distal deletions and review. Am J Med Genet A. 2007 Sep 15;143A(18):2143-9.
  3. Peltekova IT, Macdonald A, Armour CM. Microdeletion on 3p25 in a patient with features of 3p deletion syndrome. Am J Med Genet A. 2012 Oct;158A(10):2583-6.doi: 10.1002/ajmg.a.35559.
  4. Pohjola P, de Leeuw N, Penttinen M, Kääriäinen H. Terminal 3p deletions in twofamilies--correlation between molecular karyotype and phenotype. Am J Med GenetA. 2010 Feb;152A(2):441-6. doi: 10.1002/ajmg.a.33215.
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Entry Collection: MedlinePlus
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Update Date: 23 Dec 2020
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